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
- 71335-2371_1bfa8227-93bd-42e2-8051-75ec8b9f8931
- Product NDC
- 71335-2371
- Form
- TABLET
- Composition / generic term
- Propranolol Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210603
- 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 (71335-2371-1) · 71335-2371-1
- 30 TABLET in 1 BOTTLE (71335-2371-2) · 71335-2371-2
- 100 TABLET in 1 BOTTLE (71335-2371-3) · 71335-2371-3
- 60 TABLET in 1 BOTTLE (71335-2371-4) · 71335-2371-4
- 90 TABLET in 1 BOTTLE (71335-2371-5) · 71335-2371-5
- 180 TABLET in 1 BOTTLE (71335-2371-6) · 71335-2371-6
- 28 TABLET in 1 BOTTLE (71335-2371-7) · 71335-2371-7
- 10 TABLET in 1 BOTTLE (71335-2371-8) · 71335-2371-8
- 120 TABLET in 1 BOTTLE (71335-2371-9) · 71335-2371-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →