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
- 71335-1765_ebc207a3-62f9-4f11-a790-8caf04a30fea
- Product NDC
- 71335-1765
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- propranolol hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200106
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPRANOLOL HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-1) · 71335-1765-1
- 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-2) · 71335-1765-2
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-3) · 71335-1765-3
- 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-4) · 71335-1765-4
- 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-5) · 71335-1765-5
- 10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-6) · 71335-1765-6
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1765-7) · 71335-1765-7
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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