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RYZOLT
RYZOLT - 43063-241-30 - (Tramadol hydrochloride)
Drug Information of RYZOLT
| Product NDC: | 43063-241 |
| Proprietary Name: | RYZOLT |
| Non Proprietary Name: | Tramadol hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Tramadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RYZOLT
| Product NDC: | 43063-241 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA021745 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100101 |
Package Information of RYZOLT
| Package NDC: | 43063-241-30 |
| Package Description: | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-241-30) |
NDC Information of RYZOLT
| NDC Code | 43063-241-30 |
| Proprietary Name | RYZOLT |
| Package Description | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-241-30) |
| Product NDC | 43063-241 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tramadol hydrochloride |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
