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tramadol hydrochloride
tramadol hydrochloride - 63629-2868-8 - (tramadol hydrochloride)
Drug Information of tramadol hydrochloride
| Product NDC: | 63629-2868 |
| Proprietary Name: | tramadol hydrochloride |
| Non Proprietary Name: | tramadol hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; tramadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of tramadol hydrochloride
| Product NDC: | 63629-2868 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075964 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020622 |
Package Information of tramadol hydrochloride
| Package NDC: | 63629-2868-8 |
| Package Description: | 56 TABLET in 1 BOTTLE (63629-2868-8) |
NDC Information of tramadol hydrochloride
| NDC Code | 63629-2868-8 |
| Proprietary Name | tramadol hydrochloride |
| Package Description | 56 TABLET in 1 BOTTLE (63629-2868-8) |
| Product NDC | 63629-2868 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tramadol hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020622 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
