FDA NDC Directory · JSON-LD · Markdown

Amiloride Hydrochloride

NDC 63629-2114 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA070346
Dosage form / routeTABLET · ORAL
Active ingredientsAMILORIDE HYDROCHLORIDE ANHYDROUS (5 mg/1)
Marketing started19860122
Package count1

External sources

Source: openFDA. Public-domain (CC0).