# Atenolol

NDC: 42708-012
Generic name: Atenolol
Labeler / Manufacturer: QPharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19950222

FDA application: ANDA074056

## Active ingredients

- ATENOLOL: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42708-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42708-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70d7a585-7a46-4eac-b2b5-2ac5b98d9882