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Nucynta
Nucynta - 50458-817-01 - (tapentadol hydrochloride)
Drug Information of Nucynta
| Product NDC: | 50458-817 |
| Proprietary Name: | Nucynta |
| Non Proprietary Name: | tapentadol hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; tapentadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nucynta
| Product NDC: | 50458-817 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203794 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121015 |
Package Information of Nucynta
| Package NDC: | 50458-817-01 |
| Package Description: | 100 mL in 1 BOTTLE (50458-817-01) |
NDC Information of Nucynta
| NDC Code | 50458-817-01 |
| Proprietary Name | Nucynta |
| Package Description | 100 mL in 1 BOTTLE (50458-817-01) |
| Product NDC | 50458-817 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tapentadol hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | TAPENTADOL HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
