Suboxone - buprenorphine hydrochloride, naloxone hydrochloride dihydrate
Navigation: NDC > Supplier starting with: R > RECKITT BENCKISER PHARMACEUTICALS INC| Field | Value |
|---|---|
| NDC Code: | 12496-1283 |
| Proprietary Name: | Suboxone |
| Suffix: | |
| Non-Proprietary Name: | buprenorphine hydrochloride, naloxone hydrochloride dihydrate |
| Dosage Form: | TABLET |
| Method: | SUBLINGUAL |
| Original Marketing Date: | 08-10-2002 |
| End of Marketing: | 01-01-2014 |
| Category Name: | NDA |
| Application Number: | NDA020733 |
| Labeler: | RECKITT BENCKISER PHARMACEUTICALS INC |
| Substance Name: | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE |
| Active Numerator Strength: | 2; .5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| DEA Schedule: | CIII |