# Nadolol

NDC: 68001-690
Generic name: Nadolol
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260225

FDA application: ANDA201893

## Active ingredients

- NADOLOL: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-690"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-690
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f11553f1-18ec-41b0-a7ad-1c9f21ef2c9f