Palafox Pharmacy; Decision and Order, 18320-18321 [2019-08703]
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18320
Federal Register / Vol. 84, No. 83 / Tuesday, April 30, 2019 / Notices
April 9, 2018 that it would conduct full
reviews (83 FR 18347, April 26, 2018).
Notice of the scheduling of the
Commission’s reviews and of a public
hearing to be held in connection
therewith was given by posting copies
of the notice in the Office of the
Secretary, U.S. International Trade
Commission, Washington, DC, and by
publishing the notice in the Federal
Register on September 14, 2018 (83 FR
46757). Effective February 4, 2019, the
Commission revised its schedule due to
the lapse in appropriations and ensuing
cessation of Commission operations (84
FR 2926, February 8, 2019). The hearing
was held in Washington, DC, on
February 21, 2019, and all persons who
requested the opportunity were
permitted to appear in person or by
counsel.
The Commission made these
determinations pursuant to section
751(c) of the Act (19 U.S.C. 1675(c)). It
completed and filed its determinations
in these reviews on April 24, 2019. The
views of the Commission are contained
in USITC Publication 4482 (April 2019),
entitled Large Residential Washers from
Korea and Mexico: Investigation Nos.
701–TA–488 and 731–TA–1199–1200
(Review).
By order of the Commission.
Issued: April 24, 2019.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2019–08671 Filed 4–29–19; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
amozie on DSK9F9SC42PROD with NOTICES
Palafox Pharmacy; Decision and Order
On August 14, 2018, the Assistant
Administrator, Diversion Control
Division, Drug Enforcement
Administration (hereinafter, DEA or
Government), issued an Order to Show
Cause to Palafox Pharmacy (hereinafter,
Registrant), of Anthony, Texas. Order to
Show Cause (hereinafter, OSC), at 1.
The Show Cause Order proposes the
revocation of Registrant’s Certificate of
Registration on the ground that it has
‘‘no state authority to handle controlled
substances.’’ Id. (citing 21 U.S.C.
824(a)(3)).
Regarding jurisdiction, the Show
Cause Order alleges that Registrant
holds DEA Certificate of Registration
No. FP1305564 at the registered address
of 929 S Main St., Anthony, Texas
79821. OSC, at 1. The Show Cause
Order alleges that this registration
expires on March 31, 2021. Id.
VerDate Sep<11>2014
18:08 Apr 29, 2019
Jkt 247001
The substantive ground for the
proceeding, as alleged in the Show
Cause Order, is that Registrant is
‘‘currently without authority to handle
controlled substances in the State of
Texas, the state in which . . . [it] is
registered with the DEA.’’ Id. at 1–2.
Specifically, the Show Cause Order
alleges that the Texas State Board of
Pharmacy suspended Registrant’s
pharmacy license on June 18, 2018. Id.
at 1.
The Show Cause Order notifies
Registrant of its right to request a
hearing on the allegation or to submit a
written statement while waiving its
right to a hearing, the procedures for
electing each option, and the
consequences for failing to elect either
option. Id. at 2 (citing 21 CFR 1301.43).
The Show Cause Order also notifies
Registrant of the opportunity to submit
a corrective action plan. OSC, at 2–3
(citing 21 U.S.C. 824(c)(2)(C)).
Adequacy of Service
In a Declaration dated November 2,
2018, a Diversion Investigator
(hereinafter, DI), who describes herself
as being assigned to the El Paso Field
Division, states that she had the OSC
delivered to the residential address of
Registrant’s owner. Government Exhibit
(hereinafter, GX) 6 (DI Declaration), at
1–2.1 See also GX 6, at 8–10 (proof of
delivery).
In its Request for Final Agency Action
dated November 7, 2018, the
Government represents that ‘‘[a]t least
30 days have passed since the time the
. . . [OSC] was served on Registrant
. . . [and] Registrant has not requested
a hearing.’’ Request for Final Agency
Action (hereinafter, RFAA), at 1.2 The
Government seeks the issuance of ‘‘a
Final Order revoking Registrant’s DEA
registration.’’ RFAA, at 4.
Based on the DI’s Declaration, the
Government’s written representations,
and my review of the record, I find that
the Government accomplished service
on August 30, 2018.3 GX 6, at 1–2, 8–
10. I also find that more than 30 days
have passed since the date the
Government served the OSC. Further,
based on the Government’s written
representations, I find that neither
Registrant, nor anyone purporting to
1 According to the DI, delivery attempts to
Registrant’s registered address were not successful.
GX 6, at 1.
2 In its Supplement to Request for Final Agency
Action dated March 19, 2019, the Government
represents that ‘‘Registrant has not otherwise
corresponded or communicated with DEA regarding
the Order to Show Cause served on it, including the
filing of any written statement in lieu of a hearing.’’
Supplement, at 1.
3 Nasim F. Khan, M.D., 73 FR 4630, 4630 (2008);
Patrick K. Riggs, M.D., 72 FR 71,959, 71,959 (2007).
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Frm 00089
Fmt 4703
Sfmt 4703
represent him, requested a hearing,
submitted a written statement while
waiving Registrant’s right to a hearing,
or submitted a corrective action plan.
Accordingly, I find that Registrant has
waived his right to a hearing and his
right to submit a written statement and
corrective action plan. 21 CFR
1301.43(d) and 21 U.S.C. 824(c)(2)(C). I,
therefore, issue this Decision and Order
based on the record submitted by the
Government, which constitutes the
entire record before me. 21 CFR
1301.43(e).
Findings of Fact
Registrant’s DEA Registration
Registrant is the holder of DEA
Certificate of Registration No.
FP1305564 at the registered address of
929 S Main St., Anthony, Texas 79821
under the electronic signature of Samuel
Ambrosio Gurrola. GX 1 (Certification of
Registration History), at 1. Pursuant to
this registration, Registrant is authorized
to dispense controlled substances in
schedules IV and V as a retail pharmacy.
Id. Registrant’s registration expires on
March 31, 2021 and is in an active
pending status. Id.
The Status of Registrant’s State License
Registrant’s Texas pharmacy license
(number 26185) was revoked by Order
of the Texas State Board of Pharmacy.
GX 5 (Texas State Board of Pharmacy
certified ‘‘Agreed Board Order #J–18–
022–B’’ dated August 7, 2018), at 3. The
revocation was effective on the date of
entry of the Order. Id. The record
evidence shows that Registrant’s Texas
pharmacy license number 26185 is
revoked. GX 7 (Texas State Board of
Pharmacy website screen print showing
Registrant’s pharmacy license status as
‘‘Revocation’’), at 1. Further, according
to the online records of the Texas State
Board of Pharmacy, of which I take
official notice, Registrant’s pharmacy
license is still revoked.4 Texas State
Board of Pharmacy website, https://
4 Under the Administrative Procedure Act, an
agency ‘‘may take official notice of facts at any stage
in a proceeding—even in the final decision.’’
United States Department of Justice, Attorney
General’s Manual on the Administrative Procedure
Act 80 (1947) (Wm. W. Gaunt & Sons, Inc., Reprint
1979). Pursuant to 5 U.S.C. 556(e), ‘‘[w]hen an
agency decision rests on official notice of a material
fact not appearing in the evidence in the record, a
party is entitled, on timely request, to an
opportunity to show the contrary.’’ Accordingly,
Registrant may dispute my finding by filing a
properly supported motion for reconsideration
within 15 calendar days of the date of this Order.
Any such motion shall be filed with the Office of
the Administrator and a copy shall be served on the
Government. In the event Registrant files a motion,
the Government shall have 15 calendar days to file
a response.
E:\FR\FM\30APN1.SGM
30APN1
18321
Federal Register / Vol. 84, No. 83 / Tuesday, April 30, 2019 / Notices
amozie on DSK9F9SC42PROD with NOTICES
www.pharmacy.texas.gov/ (last visited
April 5, 2019).
Accordingly, I find that Registrant
currently does not have a license to
operate a pharmacy in Texas, the State
in which he is registered with the DEA.
Discussion
Pursuant to 21 U.S.C. 824(a)(3), the
Attorney General is authorized to
suspend or revoke a registration issued
under section 823 of the Controlled
Substances Act (hereinafter, CSA),
‘‘upon a finding that the registrant . . .
has had his State license or registration
suspended . . . [or] revoked . . . by
competent State authority and is no
longer authorized by State law to engage
in the . . . dispensing of controlled
substances.’’ A pharmacy is a
‘‘practitioner’’ under the CSA. 21 U.S.C.
802(21). With respect to a practitioner,
the DEA has also long held that the
possession of authority to dispense
controlled substances under the laws of
the State in which a practitioner engages
in professional practice is a
fundamental condition for obtaining
and maintaining a practitioner’s
registration. See, e.g., James L. Hooper,
M.D., 76 FR 71,371 (2011), pet. for rev.
denied, 481 Fed. Appx. 826 (4th Cir.
2012); Roots Pharmaceuticals, Inc., 76
FR 51,430 (2011); Ideal Pharmacy Care,
Inc., d/b/a Esplanade Pharmacy, 76 FR
51,415 (2011); Bourne Pharmacy, Inc.,
72 FR 18,273 (2007); Frederick Marsh
Blanton, M.D., 43 FR 27,616 (1978).
This rule derives from the text of two
provisions of the CSA. First, Congress
defined the term ‘‘practitioner’’ to mean
‘‘a physician, . . . pharmacy, . . . or
other person licensed, registered, or
otherwise permitted, by . . . the
jurisdiction in which he practices . . .,
to distribute, dispense, . . . [or]
administer . . . a controlled substance
in the course of professional practice.’’
21 U.S.C. 802(21). Second, in setting the
requirements for obtaining a
practitioner’s registration, Congress
directed that ‘‘[t]he Attorney General
shall register practitioners . . . if the
applicant is authorized to dispense . . .
controlled substances under the laws of
the State in which he practices.’’ 21
U.S.C. 823(f). Because Congress has
clearly mandated that a practitioner
possess State authority in order to be
deemed a practitioner under the CSA,
the DEA has held repeatedly that
revocation of a practitioner’s registration
is the appropriate sanction whenever he
is no longer authorized to dispense
controlled substances under the laws of
the State in which he practices. See,
e.g., James L. Hooper, supra, 76 FR at
71,371–72; Roots Pharmaceuticals, Inc.,
supra, 76 FR at 51,430; Ideal Pharmacy
VerDate Sep<11>2014
18:54 Apr 29, 2019
Jkt 247001
Care, Inc., d/b/a Esplanade Pharmacy,
supra, 76 FR at 51,416 n.1; Bourne
Pharmacy, Inc., supra, 72 FR at 18,274;
Sheran Arden Yeates, M.D., 71 FR
39,130, 39,131 (2006); Dominick A.
Ricci, M.D., 58 FR 51,104, 51,105 (1993);
Bobby Watts, M.D., 53 FR 11,919, 11,920
(1988); Frederick Marsh Blanton, supra,
43 FR at 27,617.
According to Texas statute, ‘‘A person
may not operate a pharmacy in this state
unless the pharmacy is licensed by the
board.’’ Tex. Occupations Code Ann.
§ 560.001(a) (West, Westlaw current
through the end of the 2017 Regular and
First Called Sessions of the 85th
Legislature). Further, ‘‘a person who is
not registered with or exempt from
registration with the Federal Drug
Enforcement Administration may not
manufacture, distribute, prescribe,
possess, analyze, or dispense a
controlled substance in this state.’’ 5
Tex. Health and Safety Code Ann.
§ 481.061(a) (West, Westlaw current
through the end of the 2017 Regular and
First Called Sessions of the 85th
Legislature).
The undisputed evidence in the
record before me is that Registrant
currently lacks authority to operate a
pharmacy in Texas. As such, Registrant
is not qualified to dispense controlled
substances as a ‘‘practitioner.’’ I will,
therefore, order that Registrant’s DEA
registration be revoked.
Order
Pursuant to 28 CFR 0.100(b) and the
authority vested in me by 21 U.S.C.
824(a), I order that DEA Certificate of
Registration No. FP1305564 issued to
Palafox Pharmacy be, and it hereby is,
revoked. This Order is effective May 30,
2019.
Dated: April 5, 2019.
Uttam Dhillon,
Acting Administrator.
[FR Doc. 2019–08703 Filed 4–29–19; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Application: Mylan Pharmaceuticals
Inc.
Registered bulk manufacturers of
the affected basic classes, and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before May 30, 2019. Such persons
may also file a written request for a
hearing on the application on or before
May 30, 2019.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for hearing must be
sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152. All requests for hearing
should also be sent to: (1) Drug
Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette
Drive, Springfield, Virginia 22152; and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DPW, 8701 Morrissette
Drive, Springfield, Virginia 22152.
Comments and requests for hearings on
applications to import narcotic raw
material are not appropriate. 72 FR
3417, (January 25, 2007).
SUPPLEMENTARY INFORMATION: The
Attorney General has delegated his
authority under the Controlled
Substances Act to the Administrator of
the Drug Enforcement Administration
(DEA), 28 CFR 0.100(b). Authority to
exercise all necessary functions with
respect to the promulgation and
implementation of 21 CFR part 1301,
incident to the registration of
manufacturers, distributors, dispensers,
importers, and exporters of controlled
substances (other than final orders in
connection with suspension, denial, or
revocation of registration) has been
redelegated to the Assistant
Administrator of the DEA Diversion
Control Division (‘‘Assistant
Administrator’’) pursuant to section 7 of
28 CFR part 0, appendix to subpart R.
In accordance with 21 CFR
1301.34(a), this is notice that on
November 13, 2018, Mylan
Pharmaceuticals Inc., 3711 Collins Ferry
Road, Morgantown, West Virginia 26505
applied to be registered as an importer
of the following basic classes of
controlled substances:
DATES:
Controlled substance
ACTION:
Notice of application.
5A
‘‘dispenser’’ includes a pharmacy that
dispenses a controlled substance. Tex. Health and
Safety Code Ann. § 481.002(13) (West, Westlaw
current through the end of the 2017 Regular and
First Called Sessions of the 85th Legislature).
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Methylphenidate ............
Oxycodone ....................
Hydromorphone .............
Methadone .....................
Morphine ........................
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II
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Agencies
[Federal Register Volume 84, Number 83 (Tuesday, April 30, 2019)]
[Notices]
[Pages 18320-18321]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-08703]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Palafox Pharmacy; Decision and Order
On August 14, 2018, the Assistant Administrator, Diversion Control
Division, Drug Enforcement Administration (hereinafter, DEA or
Government), issued an Order to Show Cause to Palafox Pharmacy
(hereinafter, Registrant), of Anthony, Texas. Order to Show Cause
(hereinafter, OSC), at 1. The Show Cause Order proposes the revocation
of Registrant's Certificate of Registration on the ground that it has
``no state authority to handle controlled substances.'' Id. (citing 21
U.S.C. 824(a)(3)).
Regarding jurisdiction, the Show Cause Order alleges that
Registrant holds DEA Certificate of Registration No. FP1305564 at the
registered address of 929 S Main St., Anthony, Texas 79821. OSC, at 1.
The Show Cause Order alleges that this registration expires on March
31, 2021. Id.
The substantive ground for the proceeding, as alleged in the Show
Cause Order, is that Registrant is ``currently without authority to
handle controlled substances in the State of Texas, the state in which
. . . [it] is registered with the DEA.'' Id. at 1-2. Specifically, the
Show Cause Order alleges that the Texas State Board of Pharmacy
suspended Registrant's pharmacy license on June 18, 2018. Id. at 1.
The Show Cause Order notifies Registrant of its right to request a
hearing on the allegation or to submit a written statement while
waiving its right to a hearing, the procedures for electing each
option, and the consequences for failing to elect either option. Id. at
2 (citing 21 CFR 1301.43). The Show Cause Order also notifies
Registrant of the opportunity to submit a corrective action plan. OSC,
at 2-3 (citing 21 U.S.C. 824(c)(2)(C)).
Adequacy of Service
In a Declaration dated November 2, 2018, a Diversion Investigator
(hereinafter, DI), who describes herself as being assigned to the El
Paso Field Division, states that she had the OSC delivered to the
residential address of Registrant's owner. Government Exhibit
(hereinafter, GX) 6 (DI Declaration), at 1-2.\1\ See also GX 6, at 8-10
(proof of delivery).
---------------------------------------------------------------------------
\1\ According to the DI, delivery attempts to Registrant's
registered address were not successful. GX 6, at 1.
---------------------------------------------------------------------------
In its Request for Final Agency Action dated November 7, 2018, the
Government represents that ``[a]t least 30 days have passed since the
time the . . . [OSC] was served on Registrant . . . [and] Registrant
has not requested a hearing.'' Request for Final Agency Action
(hereinafter, RFAA), at 1.\2\ The Government seeks the issuance of ``a
Final Order revoking Registrant's DEA registration.'' RFAA, at 4.
---------------------------------------------------------------------------
\2\ In its Supplement to Request for Final Agency Action dated
March 19, 2019, the Government represents that ``Registrant has not
otherwise corresponded or communicated with DEA regarding the Order
to Show Cause served on it, including the filing of any written
statement in lieu of a hearing.'' Supplement, at 1.
---------------------------------------------------------------------------
Based on the DI's Declaration, the Government's written
representations, and my review of the record, I find that the
Government accomplished service on August 30, 2018.\3\ GX 6, at 1-2, 8-
10. I also find that more than 30 days have passed since the date the
Government served the OSC. Further, based on the Government's written
representations, I find that neither Registrant, nor anyone purporting
to represent him, requested a hearing, submitted a written statement
while waiving Registrant's right to a hearing, or submitted a
corrective action plan. Accordingly, I find that Registrant has waived
his right to a hearing and his right to submit a written statement and
corrective action plan. 21 CFR 1301.43(d) and 21 U.S.C. 824(c)(2)(C).
I, therefore, issue this Decision and Order based on the record
submitted by the Government, which constitutes the entire record before
me. 21 CFR 1301.43(e).
---------------------------------------------------------------------------
\3\ Nasim F. Khan, M.D., 73 FR 4630, 4630 (2008); Patrick K.
Riggs, M.D., 72 FR 71,959, 71,959 (2007).
---------------------------------------------------------------------------
Findings of Fact
Registrant's DEA Registration
Registrant is the holder of DEA Certificate of Registration No.
FP1305564 at the registered address of 929 S Main St., Anthony, Texas
79821 under the electronic signature of Samuel Ambrosio Gurrola. GX 1
(Certification of Registration History), at 1. Pursuant to this
registration, Registrant is authorized to dispense controlled
substances in schedules IV and V as a retail pharmacy. Id. Registrant's
registration expires on March 31, 2021 and is in an active pending
status. Id.
The Status of Registrant's State License
Registrant's Texas pharmacy license (number 26185) was revoked by
Order of the Texas State Board of Pharmacy. GX 5 (Texas State Board of
Pharmacy certified ``Agreed Board Order #J-18-022-B'' dated August 7,
2018), at 3. The revocation was effective on the date of entry of the
Order. Id. The record evidence shows that Registrant's Texas pharmacy
license number 26185 is revoked. GX 7 (Texas State Board of Pharmacy
website screen print showing Registrant's pharmacy license status as
``Revocation''), at 1. Further, according to the online records of the
Texas State Board of Pharmacy, of which I take official notice,
Registrant's pharmacy license is still revoked.\4\ Texas State Board of
Pharmacy website, https://
[[Page 18321]]
www.pharmacy.texas.gov/ (last visited April 5, 2019).
---------------------------------------------------------------------------
\4\ Under the Administrative Procedure Act, an agency ``may take
official notice of facts at any stage in a proceeding--even in the
final decision.'' United States Department of Justice, Attorney
General's Manual on the Administrative Procedure Act 80 (1947) (Wm.
W. Gaunt & Sons, Inc., Reprint 1979). Pursuant to 5 U.S.C. 556(e),
``[w]hen an agency decision rests on official notice of a material
fact not appearing in the evidence in the record, a party is
entitled, on timely request, to an opportunity to show the
contrary.'' Accordingly, Registrant may dispute my finding by filing
a properly supported motion for reconsideration within 15 calendar
days of the date of this Order. Any such motion shall be filed with
the Office of the Administrator and a copy shall be served on the
Government. In the event Registrant files a motion, the Government
shall have 15 calendar days to file a response.
---------------------------------------------------------------------------
Accordingly, I find that Registrant currently does not have a
license to operate a pharmacy in Texas, the State in which he is
registered with the DEA.
Discussion
Pursuant to 21 U.S.C. 824(a)(3), the Attorney General is authorized
to suspend or revoke a registration issued under section 823 of the
Controlled Substances Act (hereinafter, CSA), ``upon a finding that the
registrant . . . has had his State license or registration suspended .
. . [or] revoked . . . by competent State authority and is no longer
authorized by State law to engage in the . . . dispensing of controlled
substances.'' A pharmacy is a ``practitioner'' under the CSA. 21 U.S.C.
802(21). With respect to a practitioner, the DEA has also long held
that the possession of authority to dispense controlled substances
under the laws of the State in which a practitioner engages in
professional practice is a fundamental condition for obtaining and
maintaining a practitioner's registration. See, e.g., James L. Hooper,
M.D., 76 FR 71,371 (2011), pet. for rev. denied, 481 Fed. Appx. 826
(4th Cir. 2012); Roots Pharmaceuticals, Inc., 76 FR 51,430 (2011);
Ideal Pharmacy Care, Inc., d/b/a Esplanade Pharmacy, 76 FR 51,415
(2011); Bourne Pharmacy, Inc., 72 FR 18,273 (2007); Frederick Marsh
Blanton, M.D., 43 FR 27,616 (1978).
This rule derives from the text of two provisions of the CSA.
First, Congress defined the term ``practitioner'' to mean ``a
physician, . . . pharmacy, . . . or other person licensed, registered,
or otherwise permitted, by . . . the jurisdiction in which he practices
. . ., to distribute, dispense, . . . [or] administer . . . a
controlled substance in the course of professional practice.'' 21
U.S.C. 802(21). Second, in setting the requirements for obtaining a
practitioner's registration, Congress directed that ``[t]he Attorney
General shall register practitioners . . . if the applicant is
authorized to dispense . . . controlled substances under the laws of
the State in which he practices.'' 21 U.S.C. 823(f). Because Congress
has clearly mandated that a practitioner possess State authority in
order to be deemed a practitioner under the CSA, the DEA has held
repeatedly that revocation of a practitioner's registration is the
appropriate sanction whenever he is no longer authorized to dispense
controlled substances under the laws of the State in which he
practices. See, e.g., James L. Hooper, supra, 76 FR at 71,371-72; Roots
Pharmaceuticals, Inc., supra, 76 FR at 51,430; Ideal Pharmacy Care,
Inc., d/b/a Esplanade Pharmacy, supra, 76 FR at 51,416 n.1; Bourne
Pharmacy, Inc., supra, 72 FR at 18,274; Sheran Arden Yeates, M.D., 71
FR 39,130, 39,131 (2006); Dominick A. Ricci, M.D., 58 FR 51,104, 51,105
(1993); Bobby Watts, M.D., 53 FR 11,919, 11,920 (1988); Frederick Marsh
Blanton, supra, 43 FR at 27,617.
According to Texas statute, ``A person may not operate a pharmacy
in this state unless the pharmacy is licensed by the board.'' Tex.
Occupations Code Ann. Sec. 560.001(a) (West, Westlaw current through
the end of the 2017 Regular and First Called Sessions of the 85th
Legislature). Further, ``a person who is not registered with or exempt
from registration with the Federal Drug Enforcement Administration may
not manufacture, distribute, prescribe, possess, analyze, or dispense a
controlled substance in this state.'' \5\ Tex. Health and Safety Code
Ann. Sec. 481.061(a) (West, Westlaw current through the end of the
2017 Regular and First Called Sessions of the 85th Legislature).
---------------------------------------------------------------------------
\5\ A ``dispenser'' includes a pharmacy that dispenses a
controlled substance. Tex. Health and Safety Code Ann. Sec.
481.002(13) (West, Westlaw current through the end of the 2017
Regular and First Called Sessions of the 85th Legislature).
---------------------------------------------------------------------------
The undisputed evidence in the record before me is that Registrant
currently lacks authority to operate a pharmacy in Texas. As such,
Registrant is not qualified to dispense controlled substances as a
``practitioner.'' I will, therefore, order that Registrant's DEA
registration be revoked.
Order
Pursuant to 28 CFR 0.100(b) and the authority vested in me by 21
U.S.C. 824(a), I order that DEA Certificate of Registration No.
FP1305564 issued to Palafox Pharmacy be, and it hereby is, revoked.
This Order is effective May 30, 2019.
Dated: April 5, 2019.
Uttam Dhillon,
Acting Administrator.
[FR Doc. 2019-08703 Filed 4-29-19; 8:45 am]
BILLING CODE 4410-09-P