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
- 71335-2594_255faee4-9699-426d-a720-b500236fb6cb
- Product NDC
- 71335-2594
- Form
- TABLET
- Composition / generic term
- Propranolol hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191031
- Source listing expiry
- 20261231
Source-listed ingredients
- PROPRANOLOL HYDROCHLORIDE — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2594-1) · 71335-2594-1
- 100 TABLET in 1 BOTTLE (71335-2594-2) · 71335-2594-2
- 90 TABLET in 1 BOTTLE (71335-2594-3) · 71335-2594-3
- 60 TABLET in 1 BOTTLE (71335-2594-4) · 71335-2594-4
- 10 TABLET in 1 BOTTLE (71335-2594-5) · 71335-2594-5
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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