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Ultram ER
Ultram ER - 50458-655-30 - (Tramadol Hydrochloride)
Drug Information of Ultram ER
| Product NDC: | 50458-655 |
| Proprietary Name: | Ultram ER |
| Non Proprietary Name: | Tramadol Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Tramadol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultram ER
| Product NDC: | 50458-655 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021692 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051001 |
Package Information of Ultram ER
| Package NDC: | 50458-655-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50458-655-30) |
NDC Information of Ultram ER
| NDC Code | 50458-655-30 |
| Proprietary Name | Ultram ER |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50458-655-30) |
| Product NDC | 50458-655 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tramadol Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20051001 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
