Additions and Modifications to the List of Drug Products That Have Been Withdrawn or Removed From the Market for Reasons of Safety or Effectiveness; Correction, 68395 [2014-27038]
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68395
Federal Register / Vol. 79, No. 221 / Monday, November 17, 2014 / Proposed Rules
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 216
[Docket No. FDA–1999–N–0194]
RIN 0910–AH08
Additions and Modifications to the List
of Drug Products That Have Been
Withdrawn or Removed From the
Market for Reasons of Safety or
Effectiveness; Correction
AGENCY:
Food and Drug Administration,
HHS.
Proposed rule; withdrawal of
previous proposed rule; correction.
ACTION:
The Food and Drug
Administration (FDA) is correcting a
document entitled ‘‘Additions and
Modifications to the List of Drug
Products That Have Been Withdrawn or
Removed From the Market for Reasons
of Safety or Effectiveness’’ that appeared
in the Federal Register of July 2, 2014.
The document proposed amending
FDA’s regulations to revise the list of
drug products that may not be
compounded under the exemptions
provided by the Federal Food, Drug, and
SUMMARY:
Cosmetic Act because the drug products
have been withdrawn or removed from
the market after the drug products or
components of such drug products were
found to be unsafe or not effective. The
document also withdrew the previous
proposed rule regarding additions to
this list (see the Federal Register of
January 4, 2000). The document was
published with an incorrect RIN
number. This document corrects the
error.
DATES: The proposed rule published
July 2, 2014 (79 FR 37687) is corrected
as of November 17, 2014.
FOR FURTHER INFORMATION CONTACT:
Edisa Gozun, Center for Drug Evaluation
and Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 51, Rm. 5199, Silver Spring,
MD 20993–0002, 301–796–3110.
SUPPLEMENTARY INFORMATION: In FR Doc.
2014–15371, appearing on page 37687
in the Federal Register of July 2, 2014
(79 FR 37687), FDA is making the
following correction:
1. On page 37687, in the first column,
the RIN number heading is corrected to
read ‘‘RIN 0910–AH08’’.
2. On page 37687, in the second
column, the RIN number under the
ADDRESSES heading is corrected to read
‘‘RIN 0910–AH08’’.
3. On page 37687, in the second
column, the RIN number under the
Instructions sub-heading is corrected to
read ‘‘RIN 0910–AH08’’.
Dated: November 10, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014–27038 Filed 11–14–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF LABOR
Mine Safety and Health Administration
30 CFR Part 100
[Docket No. MSHA–2014–0009]
RIN 1219–AB72
Criteria and Procedures for
Assessment of Civil Penalties
Correction
In proposed rule document 2014–
17935 appearing on pages 44493–44518
in the issue of July 31, 2014, make the
following correction:
Beginning on page 44497, Part 100
Table III is corrected to read as set forth
below:
PART 100 TABLE III—SIZE OF METAL/NONMETAL MINE
Existing rule
Proposed rule
Annual hours
worked at mine
(× 1,000)
Penalty points
(out of maximum
208 points)
Annual hours
worked at mine
(× 1,000)
Penalty points
(out of maximum
100 points)
0
0 to 5 ......................................................................
0
>5 to 10 ..................................................................
>10 to 20 ................................................................
>20 to 30 ................................................................
>30 to 50 ................................................................
>50 to 100 ..............................................................
>100 to 200 ............................................................
1
2
3
4
5
6
>5 to 200 ................................................................
1
>200 to 300 ............................................................
>300 to 500 ............................................................
>500 to 700 ............................................................
>700 to 1,000 .........................................................
>1,000 to 1,500 ......................................................
7
8
9
10
11
>200 to 1,500 .........................................................
2
>1,500 to 2,000 ......................................................
>2,000 to 3,000 ......................................................
12
13
>1,500 to 3,000 ......................................................
3
>3,000 to 5,000 ......................................................
>5,000 ....................................................................
mstockstill on DSK4VPTVN1PROD with PROPOSALS
0 to 5 ......................................................................
14
15
>3,000 ....................................................................
4
[FR Doc. C1–2014–17935 Filed 11–14–14; 8:45 am]
BILLING CODE 1505–01–D
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16:18 Nov 14, 2014
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Agencies
[Federal Register Volume 79, Number 221 (Monday, November 17, 2014)]
[Proposed Rules]
[Page 68395]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-27038]
[[Page 68395]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 216
[Docket No. FDA-1999-N-0194]
RIN 0910-AH08
Additions and Modifications to the List of Drug Products That
Have Been Withdrawn or Removed From the Market for Reasons of Safety or
Effectiveness; Correction
AGENCY: Food and Drug Administration, HHS.
ACTION: Proposed rule; withdrawal of previous proposed rule;
correction.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is correcting a
document entitled ``Additions and Modifications to the List of Drug
Products That Have Been Withdrawn or Removed From the Market for
Reasons of Safety or Effectiveness'' that appeared in the Federal
Register of July 2, 2014. The document proposed amending FDA's
regulations to revise the list of drug products that may not be
compounded under the exemptions provided by the Federal Food, Drug, and
Cosmetic Act because the drug products have been withdrawn or removed
from the market after the drug products or components of such drug
products were found to be unsafe or not effective. The document also
withdrew the previous proposed rule regarding additions to this list
(see the Federal Register of January 4, 2000). The document was
published with an incorrect RIN number. This document corrects the
error.
DATES: The proposed rule published July 2, 2014 (79 FR 37687) is
corrected as of November 17, 2014.
FOR FURTHER INFORMATION CONTACT: Edisa Gozun, Center for Drug
Evaluation and Research, Food and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 5199, Silver Spring, MD 20993-0002, 301-
796-3110.
SUPPLEMENTARY INFORMATION: In FR Doc. 2014-15371, appearing on page
37687 in the Federal Register of July 2, 2014 (79 FR 37687), FDA is
making the following correction:
1. On page 37687, in the first column, the RIN number heading is
corrected to read ``RIN 0910-AH08''.
2. On page 37687, in the second column, the RIN number under the
ADDRESSES heading is corrected to read ``RIN 0910-AH08''.
3. On page 37687, in the second column, the RIN number under the
Instructions sub-heading is corrected to read ``RIN 0910-AH08''.
Dated: November 10, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-27038 Filed 11-14-14; 8:45 am]
BILLING CODE 4164-01-P