United States · FDA National Drug Code directory
Buprenorphine HCl
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
- 71335-1163_4ee49cc8-55ca-4274-9ea6-70d7891d8853
- Product NDC
- 71335-1163
- Form
- TABLET
- Composition / generic term
- Buprenorphine HCl
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091008
- Source listing expiry
- 20261231
Source-listed ingredients
- BUPRENORPHINE HYDROCHLORIDE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (71335-1163-0) · 71335-1163-0
- 90 TABLET in 1 BOTTLE (71335-1163-1) · 71335-1163-1
- 60 TABLET in 1 BOTTLE (71335-1163-2) · 71335-1163-2
- 30 TABLET in 1 BOTTLE (71335-1163-3) · 71335-1163-3
- 20 TABLET in 1 BOTTLE (71335-1163-4) · 71335-1163-4
- 7 TABLET in 1 BOTTLE (71335-1163-5) · 71335-1163-5
- 28 TABLET in 1 BOTTLE (71335-1163-6) · 71335-1163-6
- 1 TABLET in 1 BOTTLE (71335-1163-7) · 71335-1163-7
- 12 TABLET in 1 BOTTLE (71335-1163-8) · 71335-1163-8
- 14 TABLET in 1 BOTTLE (71335-1163-9) · 71335-1163-9
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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