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Tramadol ER
Tramadol ER - 16590-893-30 - (Tramadol ER)
Drug Information of Tramadol ER
| Product NDC: | 16590-893 |
| Proprietary Name: | Tramadol ER |
| Non Proprietary Name: | Tramadol ER |
| Active Ingredient(s): | 200 mg/1 & nbsp; Tramadol ER |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tramadol ER
| Product NDC: | 16590-893 |
| Labeler Name: | Stat Rx USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078783 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091027 |
Package Information of Tramadol ER
| Package NDC: | 16590-893-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-893-30) |
NDC Information of Tramadol ER
| NDC Code | 16590-893-30 |
| Proprietary Name | Tramadol ER |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-893-30) |
| Product NDC | 16590-893 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tramadol ER |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091027 |
| Marketing Category Name | ANDA |
| Labeler Name | Stat Rx USA |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
