FDA NDC Directory · JSON-LD · Markdown

Amiloride Hydrochloride and Hydrochlorothiazide

NDC 0555-0483 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071111
Dosage form / routeTABLET · ORAL
Active ingredientsAMILORIDE HYDROCHLORIDE (5 mg/1)
HYDROCHLOROTHIAZIDE (50 mg/1)
Marketing started19891201
Package count2

External sources

Source: openFDA. Public-domain (CC0).