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Atenolol

NDC 65862-170 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078512
Dosage form / routeTABLET · ORAL
Active ingredientsATENOLOL (100 mg/1)
Marketing started20071031
Package count2

External sources

Source: openFDA. Public-domain (CC0).