| NDC Code | 67046-991-30 |
|---|
| Package Description | 30 TABLET in 1 BLISTER PACK (67046-991-30) |
|---|
| Product NDC | 67046-991 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Buprenorphine Hydrochloride |
|---|
| Non-Proprietary Name | Buprenorphine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | SUBLINGUAL |
|---|
| Start Marketing Date | 20100924 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090622 |
|---|
| Manufacturer | Contract Pharmacy Services-PA |
|---|
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
|---|
| Strength | 8 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Partial Opioid Agonists [MoA],Partial Opioid Agonist [EPC] |
|---|
| DEA Schedule | CIII |
|---|