MIDODRINE HYDROCHLORIDE

Generic: MIDODRINE HYDROCHLORIDE

Mylan Pharmaceuticals Inc.Manufacturer

ORALRoute

MIDODRINE HYDROCHLORIDEActive Substance

2003-09-10Original Approval

MIDODRINE HYDROCHLORIDE is FDA application ANDA076577, sponsored by MYLAN PHARMS INC. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.

Recalls

Class II2026-02-17

Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Maj

Defective container; inadequately sealed blister packaging.