# Nadolol

NDC: 68001-632
Generic name: Nadolol
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250107

FDA application: ANDA210955

## Active ingredients

- NADOLOL: 80 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-632"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-632
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15822faf-6924-4a63-a4e1-6058b308708c