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ULTRAM
ULTRAM - 49999-022-20 - (tramadol hydrochloride)
Drug Information of ULTRAM
| Product NDC: | 49999-022 |
| Proprietary Name: | ULTRAM |
| Non Proprietary Name: | tramadol hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; tramadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRAM
| Product NDC: | 49999-022 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020281 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120320 |
Package Information of ULTRAM
| Package NDC: | 49999-022-20 |
| Package Description: | 20 TABLET, COATED in 1 BOTTLE (49999-022-20) |
NDC Information of ULTRAM
| NDC Code | 49999-022-20 |
| Proprietary Name | ULTRAM |
| Package Description | 20 TABLET, COATED in 1 BOTTLE (49999-022-20) |
| Product NDC | 49999-022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tramadol hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120320 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
