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
- 70069-027_abc53fa8-3d75-47b5-bfb1-d61872c1ddb4
- Product NDC
- 70069-027
- Form
- INJECTION
- Composition / generic term
- Buprenorphine Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250211
- 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 (70069-027-05) / 1 mL in 1 VIAL · 70069-027-05
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 →