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
- 51991-819_f7b4203a-c93c-47a2-9ad0-41df7d7a2c26
- Product NDC
- 51991-819
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- propranolol hydrochloride
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130311
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPRANOLOL HYDROCHLORIDE — 120 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-819-01) · 51991-819-01
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-819-05) · 51991-819-05
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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