# Propranolol Hydrochloride

NDC: 82619-134
Generic name: Propranolol Hydrochloride
Labeler / Manufacturer: Creekwood Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260829

FDA application: ANDA219460

## Active ingredients

- PROPRANOLOL HYDROCHLORIDE: 120 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82619-134"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82619-134
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=289f39f4-ebd3-4fd9-bbb3-72de8124795a