FDA NDC Directory · JSON-LD · Markdown

Midodrine Hydrochloride

NDC 85293-005 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUmasuto, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207613
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (2.5 mg/1)
Marketing started20250305
Package count1

External sources

Source: openFDA. Public-domain (CC0).