Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution

ICR 199803-0910-003

OMB: 0910-0045

Federal Form Document

Forms and Documents
Document
Name
Status
No forms / supporting documents in this ICR. Check IC Document Collections.
IC Document Collections
ICR Details
0910-0045 199803-0910-003
Historical Active 199406-0910-001
HHS/FDA
Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution
Reinstatement with change of a previously approved collection   No
Regular
Approved without change 04/27/1998
Retrieve Notice of Action (NOA) 03/12/1998
  Inventory as of this Action Requested Previously Approved
07/31/2001 07/31/2001
62,700 0 0
40,383 0 0
0 0 0

Manufacturers must submit reports to FDA and keep records pertaining to registering their establishments and listing their drug products with FDA.

None
None


No

1
IC Title Form No. Form Name
Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution 2656, 2656(E), 2657, 2658

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 62,700 0 0 62,700 0 0
Annual Time Burden (Hours) 40,383 0 0 40,383 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
No

$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
03/12/1998


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