United States · FDA National Drug Code directory

Propranolol Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 63629-2281_71538bf0-1d4c-4d11-8aaa-2e09e168327e
Product NDC: 63629-2281
Form: TABLET
Composition / generic term: propranolol hydrochloride
Labeler: Bryant Ranch Prepack
Marketing category: ANDA
Marketing start / end (source format): 20100621
Source listing expiry: 20261231

Source-listed ingredients

PROPRANOLOL HYDROCHLORIDE — 80 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (63629-2281-1) · 63629-2281-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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