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RYZOLT
RYZOLT - 16590-253-90 - (TRAMADOL HYDROCHLORIDE)
Drug Information of RYZOLT
| Product NDC: | 16590-253 |
| Proprietary Name: | RYZOLT |
| 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 RYZOLT
| Product NDC: | 16590-253 |
| Labeler Name: | Stat Rx USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021745 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081230 |
Package Information of RYZOLT
| Package NDC: | 16590-253-90 |
| Package Description: | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-253-90) |
NDC Information of RYZOLT
| NDC Code | 16590-253-90 |
| Proprietary Name | RYZOLT |
| Package Description | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (16590-253-90) |
| Product NDC | 16590-253 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRAMADOL HYDROCHLORIDE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | NDA |
| Labeler Name | Stat Rx USA |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
