NDC Code | 54569-6578-0 |
Package Description | 30 TABLET in 1 BOTTLE (54569-6578-0) |
Product NDC | 54569-6578 |
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 | A-S Medication Solutions LLC |
Substance Name | BUPRENORPHINE HYDROCHLORIDE |
Strength | 8 |
Strength Unit | mg/1 |
Pharmacy Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
DEA Schedule | CIII |