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Losartan Potassium and Hydrochlorothiazide

NDC 62332-048 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091617
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
LOSARTAN POTASSIUM (50 mg/1)
Marketing started20160523
Package count4

External sources

Source: openFDA. Public-domain (CC0).