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Losartan Potassium

NDC 65841-730 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078243
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLOSARTAN POTASSIUM (50 mg/1)
Marketing started20101004
Package count5

External sources

Source: openFDA. Public-domain (CC0).