NDC Code | 54868-5707-0 |
Package Description | 30 TABLET in 1 BOTTLE (54868-5707-0) |
Product NDC | 54868-5707 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Suboxone |
Non-Proprietary Name | Buprenorphine Hydrochloride And Naloxone Hydrochloride |
Dosage Form | TABLET |
Usage | SUBLINGUAL |
Start Marketing Date | 20080707 |
Marketing Category Name | NDA |
Application Number | NDA020733 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
Strength | 8; 2 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
DEA Schedule | CIII |