FDA NDC Directory · JSON-LD · Markdown

Amiloride Hydrochloride

NDC 42794-005 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSigmapharm Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079133
Dosage form / routeTABLET · ORAL
Active ingredientsAMILORIDE HYDROCHLORIDE ANHYDROUS (5 mg/1)
Marketing started20210614
Package count1

External sources

Source: openFDA. Public-domain (CC0).