Buprenorphine Hydrochloride 00143-9246
Product NDC
00143-9246- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- May 25, 2005
- Listing Expires
- December 31, 2026
- Application
- ANDA076931
Active Ingredients
| Ingredient | Strength |
|---|---|
| Buprenorphine Hydrochloride | .324 mg/mL |
Drug Class
Partial Opioid Agonist [EPC]Partial Opioid Agonists [MoA]
Packaging Options(1)
5 VIAL in 1 CARTON (0143-9246-05) / 1 mL in 1 VIAL (0143-9246-01)