Consultation with FDA and Termination of Notification - Manufacturers and Repackagers

Implementation of the Drug Supply Chain Security Act - Identification of Suspect Product and Notification

OMB: 0910-0806

IC ID: 218217

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Consultation with FDA and Termination of Notification - Manufacturers and Repackagers CDER
 
No Modified
 
Mandatory
 

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability

Health Consumer Health and Safety

 

150 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 150 0 0 -650 0 800
Annual IC Time Burden (Hours) 150 0 0 -650 0 800
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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