FDA NDC Directory · JSON-LD · Markdown

Losartan potassium and Hydrochlorothiazide

NDC 33342-050 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202289
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
LOSARTAN POTASSIUM (50 mg/1)
Marketing started20120910
Package count4

External sources

Source: openFDA. Public-domain (CC0).