# Propranolol Hydrochloride

NDC: 70518-3552
Generic name: propranolol hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20221009

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:"70518-3552"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3552
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=414c4b69-38a1-4220-bec8-204c9a624b85