95-28520. Prescription Drug Product Labeling; Medication Guide Requirements; Extension of Comment Period  

  • [Federal Register Volume 60, Number 226 (Friday, November 24, 1995)]
    [Proposed Rules]
    [Page 58025]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-28520]
    
    
    
    =======================================================================
    -----------------------------------------------------------------------
    
    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Parts 201, 208, 314, and 601
    
    [Docket No. 93N-0371]
    RIN 0910-AA37
    
    
    Prescription Drug Product Labeling; Medication Guide 
    Requirements; Extension of Comment Period
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Proposed rule; extension of comment period.
    
    -----------------------------------------------------------------------
    
    SUMMARY: The Food and Drug Administration (FDA) is extending to 
    December 22, 1995, the comment period for the proposed rule for 
    Prescription Drug Product Labeling; Medication Guide Requirements, 
    which appeared in the Federal Register of August 24, 1995 (60 FR 
    44182). FDA is taking this action in response to several requests for 
    an extension of the comment period.
    
    DATES: Written comments by December 22, 1995.
    
    ADDRESSES: Submit written comments to the Dockets Management Branch 
    (HFA-305), Food and Drug Administration, 12420 Parklawn Dr., rm. 1-23, 
    Rockville, MD 20857.
    
    FOR FURTHER INFORMATION CONTACT: Louis A. Morris, Center for Drug 
    Evaluation and Research (HFD-240), Food and Drug Administration, 5600 
    Fishers Lane, Rockville, MD 20857, 301-594-6818.
    
    SUPPLEMENTARY INFORMATION: In the Federal Register of August 24, 1995 
    (60 FR 44182), FDA published a proposed rule for Prescription Drug 
    Product Labeling; Medication Guide Requirements. Interested persons 
    were given until November 22, 1995, to submit comments on the proposal. 
    In response to the proposal, FDA received several requests for an 
    extension of the comment period for an additional 90 days. Requestors 
    specified that this extension would allow sufficient time to adequately 
    review and analyze the proposal by various organization members, in 
    order to formulate and submit comments. After careful consideration, 
    FDA is granting a 30-day extension. Accordingly, the comment period is 
    extended to December 22, 1995.
        Interested persons may, on or before December 22, 1995, submit to 
    the Dockets Management Branch (address above) written comments 
    regarding the proposal. Two copies of any comments are to be submitted, 
    except that individuals may submit one copy. Comments are to be 
    identified with the docket number found in brackets in the heading of 
    this document. Received comments may be seen in the office above 
    between 9 a.m. and 4 p.m., Monday through Friday.
    
        Dated: November 13, 1995.
    William K. Hubbard,
    Acting Deputy Commissioner for Policy.
    [FR Doc. 95-28520 Filed 11-22-95; 8:45 am]
    BILLING CODE 4160-01-F
    
    

Document Information

Published:
11/24/1995
Department:
Food and Drug Administration
Entry Type:
Proposed Rule
Action:
Proposed rule; extension of comment period.
Document Number:
95-28520
Dates:
Written comments by December 22, 1995.
Pages:
58025-58025 (1 pages)
Docket Numbers:
Docket No. 93N-0371
RINs:
0910-AA37: Prescription Drug Product Labeling; Medication Guide
RIN Links:
https://www.federalregister.gov/regulations/0910-AA37/prescription-drug-product-labeling-medication-guide
PDF File:
95-28520.pdf
CFR: (4)
21 CFR 201
21 CFR 208
21 CFR 314
21 CFR 601