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: 50090-1501_b566cbe1-2d29-4d46-bd9c-316e363c9174
Product NDC: 50090-1501
Form: CAPSULE, EXTENDED RELEASE
Composition / generic term: propranolol hydrochloride
Labeler: A-S Medication Solutions
Marketing category: ANDA
Marketing start / end (source format): 20130311
Source listing expiry: 20261231

Source-listed ingredients

PROPRANOLOL HYDROCHLORIDE — 80 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-1501-0) · 50090-1501-0

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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