FDA NDC Directory · JSON-LD · Markdown

Midodrine Hydrochloride

NDC 52817-324 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTruPharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212543
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (5 mg/1)
Marketing started20190819
Package count1

External sources

Source: openFDA. Public-domain (CC0).