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rizatriptan benzoate
rizatriptan benzoate - 68462-467-74 - (rizatriptan benzoate)
Drug Information of rizatriptan benzoate
| Product NDC: | 68462-467 |
| Proprietary Name: | rizatriptan benzoate |
| Non Proprietary Name: | rizatriptan benzoate |
| Active Ingredient(s): | 5 mg/1 & nbsp; rizatriptan benzoate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of rizatriptan benzoate
| Product NDC: | 68462-467 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201914 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130701 |
Package Information of rizatriptan benzoate
| Package NDC: | 68462-467-74 |
| Package Description: | 4 BOX in 1 CARTON (68462-467-74) > 3 POUCH in 1 BOX > 1 BLISTER PACK in 1 POUCH > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of rizatriptan benzoate
| NDC Code | 68462-467-74 |
| Proprietary Name | rizatriptan benzoate |
| Package Description | 4 BOX in 1 CARTON (68462-467-74) > 3 POUCH in 1 BOX > 1 BLISTER PACK in 1 POUCH > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 68462-467 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rizatriptan benzoate |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | RIZATRIPTAN BENZOATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
