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Ultram
Ultram - 35356-055-30 - (Tramadol Hydrochloride)
Drug Information of Ultram
| Product NDC: | 35356-055 |
| Proprietary Name: | Ultram |
| Non Proprietary Name: | Tramadol Hydrochloride |
| Active Ingredient(s): | 100 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
| Product NDC: | 35356-055 |
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021692 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111227 |
Package Information of Ultram
| Package NDC: | 35356-055-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-055-30) |
NDC Information of Ultram
| NDC Code | 35356-055-30 |
| Proprietary Name | Ultram |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-055-30) |
| Product NDC | 35356-055 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tramadol Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111227 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
