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Atenolol

NDC 0093-0787 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074056
Dosage form / routeTABLET · ORAL
Active ingredientsATENOLOL (25 mg/1)
Marketing started20041116
Package count2

External sources

Source: openFDA. Public-domain (CC0).