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Rybix
Rybix - 59630-825-03 - (tramadol hydrochloride)
Drug Information of Rybix
| Product NDC: | 59630-825 |
| Proprietary Name: | Rybix |
| Non Proprietary Name: | tramadol hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; tramadol hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rybix
| Product NDC: | 59630-825 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021693 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050505 |
Package Information of Rybix
| Package NDC: | 59630-825-03 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (59630-825-03) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of Rybix
| NDC Code | 59630-825-03 |
| Proprietary Name | Rybix |
| Package Description | 5 BLISTER PACK in 1 CARTON (59630-825-03) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 59630-825 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tramadol hydrochloride |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20050505 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi Inc. |
| Substance Name | TRAMADOL HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
