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suboxone
suboxone - 63629-4034-3 - (buprenorphine hydrochloride and naloxone hydrochloride)
Drug Information of suboxone
| Product NDC: | 63629-4034 |
| Proprietary Name: | suboxone |
| Non Proprietary Name: | buprenorphine hydrochloride and naloxone hydrochloride |
| Active Ingredient(s): | 8; 2 mg/1; mg/1 & nbsp; buprenorphine hydrochloride and naloxone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of suboxone
| Product NDC: | 63629-4034 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020733 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090723 |
Package Information of suboxone
| Package NDC: | 63629-4034-3 |
| Package Description: | 20 TABLET in 1 BOTTLE (63629-4034-3) |
NDC Information of suboxone
| NDC Code | 63629-4034-3 |
| Proprietary Name | suboxone |
| Package Description | 20 TABLET in 1 BOTTLE (63629-4034-3) |
| Product NDC | 63629-4034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | buprenorphine hydrochloride and naloxone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090723 |
| Marketing Category Name | NDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| Strength Number | 8; 2 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
