| NDC Code | 0143-9246-05 |
|---|
| Package Description | 5 VIAL in 1 CARTON (0143-9246-05) / 1 mL in 1 VIAL (0143-9246-01) |
|---|
| Product NDC | 0143-9246 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Buprenorphine Hydrochloride |
|---|
| Non-Proprietary Name | Buprenorphine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20050525 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076931 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
|---|
| Strength | .324 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA] |
|---|
| DEA Schedule | CIII |
|---|