Safety Labeling Changes (Section 505(o)(4) of the FD&C Act)-- Rebuttal Statemen

Labeling Requirements for Human Prescription Drug and Biological Products

OMB: 0910-0572

IC ID: 251544

Information Collection (IC) Details

View Information Collection (IC)

Safety Labeling Changes (Section 505(o)(4) of the FD&C Act)-- Rebuttal Statemen
 
No New
 
Voluntary
 
21 CFR 601 21 CFR 314

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Instruction GFI_Safety Labeling Changes —Implementation of Section 505(o)(4) of the FD&C Act.pdf https://www.fda.gov/regulatory-information/search-fda-guidance-documents/safety-labeling-changes-implementation-section-505o4-federal-food-drug-and-cosmetic-act Yes Yes Printable Only

Health Consumer Health and Safety

 

36 0
   
Private Sector Businesses or other for-profits
 
   100 %

  Approved Program Change Due to New Statute Program Change Due to Agency Discretion Change Due to Adjustment in Agency Estimate Change Due to Potential Violation of the PRA Previously Approved
Annual Number of Responses for this IC 36 0 0 36 0 0
Annual IC Time Burden (Hours) 216 0 0 216 0 0
Annual IC Cost Burden (Dollars) 16,200 0 0 16,200 0 0

Title Document Date Uploaded
No associated records found
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.

© 2024 OMB.report | Privacy Policy