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
- 71335-0082_5b7d1148-a500-43c2-aefd-b8ac3aa2e6bc
- Product NDC
- 71335-0082
- 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 — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (71335-0082-1) · 71335-0082-1
- 30 TABLET in 1 BOTTLE (71335-0082-2) · 71335-0082-2
- 100 TABLET in 1 BOTTLE (71335-0082-3) · 71335-0082-3
- 60 TABLET in 1 BOTTLE (71335-0082-4) · 71335-0082-4
- 90 TABLET in 1 BOTTLE (71335-0082-5) · 71335-0082-5
- 180 TABLET in 1 BOTTLE (71335-0082-6) · 71335-0082-6
- 28 TABLET in 1 BOTTLE (71335-0082-7) · 71335-0082-7
- 10 TABLET in 1 BOTTLE (71335-0082-8) · 71335-0082-8
- 120 TABLET in 1 BOTTLE (71335-0082-9) · 71335-0082-9
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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