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Telmisartan and Hydrochlorothiazide

NDC 65862-976 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208727
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROCHLOROTHIAZIDE (12.5 mg/1)
TELMISARTAN (40 mg/1)
Marketing started20161215
Package count1

External sources

Source: openFDA. Public-domain (CC0).