Posted from: Monday, December 10, 2018 - 11:01 AM - Present

Brand Medications with Generic Alternatives Anticipated to be Approved in December


Adverse reactions or quality problems experienced with the use of a recalled product may be reported to the FDA’s MedWatch Adverse Event Reporting Program either online, by U.S. mail or by fax.

1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178


Last Updated Monday, September 16, 2019 - 08:15 AM.