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Buprenorphine hydrochloride
Buprenorphine hydrochloride - 63629-4092-1 - (Buprenorphine hydrochloride)
Drug Information of Buprenorphine hydrochloride
| Product NDC: | 63629-4092 |
| Proprietary Name: | Buprenorphine hydrochloride |
| Non Proprietary Name: | Buprenorphine hydrochloride |
| Active Ingredient(s): | 8 mg/1 & nbsp; Buprenorphine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Buprenorphine hydrochloride
| Product NDC: | 63629-4092 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA020732 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091009 |
Package Information of Buprenorphine hydrochloride
| Package NDC: | 63629-4092-1 |
| Package Description: | 10 TABLET in 1 BOTTLE (63629-4092-1) |
NDC Information of Buprenorphine hydrochloride
| NDC Code | 63629-4092-1 |
| Proprietary Name | Buprenorphine hydrochloride |
| Package Description | 10 TABLET in 1 BOTTLE (63629-4092-1) |
| Product NDC | 63629-4092 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Buprenorphine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091009 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
| Strength Number | 8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
