# Propranolol Hydrochloride

NDC: 43353-961
Generic name: propranolol hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
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: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43353-961"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43353-961
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7da9bb37-cc22-4eff-8de0-429f64cb599e