United States · FDA National Drug Code directory
Buprenorphine 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
- 0143-9246_8ba9787c-d429-4a5d-8424-e13be15cb9f1
- Product NDC
- 0143-9246
- Form
- INJECTION
- Composition / generic term
- Buprenorphine Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050525
- Source listing expiry
- 20261231
Source-listed ingredients
- BUPRENORPHINE HYDROCHLORIDE — .324 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL in 1 CARTON (0143-9246-05) / 1 mL in 1 VIAL (0143-9246-01) · 0143-9246-05
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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