eLaws
|
eCases
|
United States Code
|
Federal Courts
|
Sign In
Sign Up
eLaws
eCases »
United States Code
Federal Courts »
Home
»
Rulemaking
» Draft Guidances for Industry: Generic Drug User Fee Amendments of 2012, Questions and Answers
Draft Guidances for Industry: Generic Drug User Fee Amendments of 2012, Questions and Answers
Document ID:
FDA-2012-D-0880-0001
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
2012-20944
View Document:
Details Information
Document Subtype:
Notice of Availability
Received Date:
August 27 2012, at 12:00 AM Eastern Daylight Time
Start-End Page:
51814 - 51814
Page Count:
1
Comment Start Date:
August 27 2012, at 12:00 AM Eastern Standard Time
Comment Due Date:
October 26 2012, at 11:59 PM Eastern Standard Time
Comments
Total:
2
Generic Pharmaceutical Associations (GPhA) - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0880-0003
Comment Period Closed
Oct 26,2012 11:59 PM ET
Academy of Managed Care Pharmacy (AMCP) - Comment
Posted:
10/02/2012
ID:
FDA-2012-D-0880-0004
Comment Period Closed
Oct 26,2012 11:59 PM ET
Related Documents
Total:
0
No documents available.
Draft Guidances for Industry: Generic Drug User Fee Amendments of 2012, Questions and Answers
Details Information
Comments
Posted: 10/02/2012 ID: FDA-2012-D-0880-0003
Oct 26,2012 11:59 PM ET
Posted: 10/02/2012 ID: FDA-2012-D-0880-0004
Oct 26,2012 11:59 PM ET
Related Documents