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Submitted by Anonymous (not verified) on Thu, 09/22/2016 - 09:19
Publish Date
Review Date
Last Reviewed Date
Next Review Date
5 Years
Short Title
MedWatch: Information and Adverse Event Reporting Program - Voluntary
Detailed Description
MedWatch: Information and Adverse Event Reporting Program - Voluntary
Short Description
MedWatch: Information and Adverse Event Reporting Program - Voluntary
Site Structure
Source Organization
Download Type
Form Name
MedWatch: Information and Adverse Event Reporting Program - Voluntary (HTML)
Form ID
3500
Form Issue Date
OMB Form Approval
0910-0291
Interactive Form
Off
Bulk Approved
Off
Display Short Description
Off
Old URL
https://www.fda.gov/downloads/AboutFDA/ReportsManualsForms/Forms/UCM522074.htm
Contact
CDER Drug Info: (888) 463-633
Author
eaw
Contact

CDER Drug Info: (888) 463-6332