# Propranolol Hydrochloride

NDC: 0527-4117
Generic name: propranolol hydrochloride
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200106

FDA application: ANDA212026

## Active ingredients

- PROPRANOLOL HYDROCHLORIDE: 80 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-4117"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-4117
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5229b561-287b-463c-8679-cda4c34f440b