eLaws | eCases | United States Code | Federal Courts |
Home » Rulemaking » Guidance for Industry on Labeling for Human Prescription Drug and Biological Products; Availability: Implementing the Physician Labeling Rule Content and Format Requirements; Availability

Guidance for Industry on Labeling for Human Prescription Drug and Biological Products; Availability: Implementing the Physician Labeling Rule Content and Format Requirements; Availability

Document ID: FDA-2005-D-0153-0004
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: 2013-04195
View Document:  View as format pdf View as format html

Details Information

Document Subtype: Notice of Availability
Received Date: February 25 2013, at 12:00 AM Eastern Standard Time
Start-End Page: 12760 - 12761
Page Count: 2
Comment Start Date: February 25 2013, at 12:00 AM Eastern Standard Time

Comments

Total: 0
No comments posted.

Related Documents

Total: 0
No documents available.