NDC 70069-027 – Buprenorphine Hydrochloride
Buprenorphine Hydrochloride .324 mg/mL · Injection · Intramuscular, Intravenous
Product NDC70069-027
Product details
- Brand name
- Buprenorphine Hydrochloride
- Generic name
- Buprenorphine Hydrochloride
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- Injection
- Route
- Intramuscular, Intravenous
- Marketing category
- ANDA · ANDA219302
- Marketed since
- February 11, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride .324 mg/mL
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70069-027-05 | 5 VIAL in 1 CARTON (70069-027-05) / 1 mL in 1 VIAL | Feb 11, 2025 |
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