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LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

NDC 70010-188 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218015
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
LOSARTAN POTASSIUM (100 mg/1)
Marketing started20230929
Package count2

External sources

Source: openFDA. Public-domain (CC0).