FDA NDC Directory · JSON-LD · Markdown

Atenolol

NDC 68788-7616 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077443
Dosage form / routeTABLET · ORAL
Active ingredientsATENOLOL (50 mg/1)
Marketing started20200207
Package count4

External sources

Source: openFDA. Public-domain (CC0).