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Desvenlafaxine
Desvenlafaxine - 63304-192-30 - (Desvenlafaxine)
Drug Information of Desvenlafaxine
| Product NDC: | 63304-192 |
| Proprietary Name: | Desvenlafaxine |
| Non Proprietary Name: | Desvenlafaxine |
| Active Ingredient(s): | 100 mg/1 & nbsp; Desvenlafaxine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desvenlafaxine
| Product NDC: | 63304-192 |
| Labeler Name: | Ranbaxy Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA204150 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130305 |
Package Information of Desvenlafaxine
| Package NDC: | 63304-192-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30) |
NDC Information of Desvenlafaxine
| NDC Code | 63304-192-30 |
| Proprietary Name | Desvenlafaxine |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30) |
| Product NDC | 63304-192 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desvenlafaxine |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130305 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Pharmaceuticals Inc. |
| Substance Name | DESVENLAFAXINE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
