# Propranolol Hydrochloride

NDC: 0378-0182
Generic name: propranolol hydrochloride
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19851119

FDA application: ANDA070213

## Active ingredients

- PROPRANOLOL HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-0182"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-0182
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b94dcec7-7633-4a33-9cea-48161adeaf93