FDA NDC Directory · JSON-LD · Markdown

Midodrine Hydrochloride

NDC 0904-7642 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA217271
Dosage form / routeTABLET · ORAL
Active ingredientsMIDODRINE HYDROCHLORIDE (10 mg/1)
Marketing started20260901
Package count1

External sources

Source: openFDA. Public-domain (CC0).