Buprenorphine Hydrochloride 42023-0179
Product NDC
42023-0179- Manufacturer
- Par Health Usa, Llc
- Dosage Form
- Injection
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- July 30, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA206586
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 (42023-179-05) / 1 mL in 1 VIAL