# propranolol hydrochloride

NDC: 82804-072
Generic name: propranolol hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130311

FDA application: ANDA078703

## Active ingredients

- PROPRANOLOL HYDROCHLORIDE: 60 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d7c1de3-3cf4-4b1e-bdcc-55f423c88001