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Suboxone
Suboxone - 12496-1212-3 - (buprenorphine hydrochloride, naloxone hydrochloride)
Drug Information of Suboxone
| Product NDC: | 12496-1212 |
| Proprietary Name: | Suboxone |
| Non Proprietary Name: | buprenorphine hydrochloride, naloxone hydrochloride |
| Active Ingredient(s): | 12; 3 mg/1; mg/1 & nbsp; buprenorphine hydrochloride, naloxone hydrochloride |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | FILM, SOLUBLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Suboxone
| Product NDC: | 12496-1212 |
| Labeler Name: | Reckitt Benckiser Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022410 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120824 |
Package Information of Suboxone
| Package NDC: | 12496-1212-3 |
| Package Description: | 30 POUCH in 1 CARTON (12496-1212-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1) |
NDC Information of Suboxone
| NDC Code | 12496-1212-3 |
| Proprietary Name | Suboxone |
| Package Description | 30 POUCH in 1 CARTON (12496-1212-3) > 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1) |
| Product NDC | 12496-1212 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | buprenorphine hydrochloride, naloxone hydrochloride |
| Dosage Form Name | FILM, SOLUBLE |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20120824 |
| Marketing Category Name | NDA |
| Labeler Name | Reckitt Benckiser Pharmaceuticals Inc |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| Strength Number | 12; 3 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
