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Losartan Potassium and Hydrochlorothiazide

NDC 68788-8510 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078245
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
LOSARTAN POTASSIUM (50 mg/1)
Marketing started20230822
Package count4

External sources

Source: openFDA. Public-domain (CC0).