NDC Code | 67296-1877-9 |
Package Description | 9 FILM in 1 BOTTLE (67296-1877-9) |
Product NDC | 67296-1877 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Buprenorphine And Naloxone |
Non-Proprietary Name | Buprenorphine And Naloxone |
Dosage Form | FILM |
Usage | BUCCAL; SUBLINGUAL |
Start Marketing Date | 20190220 |
Marketing Category Name | ANDA |
Application Number | ANDA207607 |
Manufacturer | Redpharm drug |
Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE |
Strength | 8; 2 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Opioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA] |
DEA Schedule | CIII |