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Lisinopril

NDC 65862-042 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077622
Dosage form / routeTABLET · ORAL
Active ingredientsLISINOPRIL (40 mg/1)
Marketing started20060222
Package count5

External sources

Source: openFDA. Public-domain (CC0).