FDA NDC Directory · JSON-LD · Markdown

Midodrine Hydrochloride

NDC 49884-849 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207169
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (5 mg/1)
Marketing started20181029
Package count1

External sources

Source: openFDA. Public-domain (CC0).