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Rizatriptan Benzoate
Rizatriptan Benzoate - 0378-3701-56 - (rizatriptan benzoate)
Drug Information of Rizatriptan Benzoate
| Product NDC: | 0378-3701 |
| 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: | 0378-3701 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078173 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121231 |
Package Information of Rizatriptan Benzoate
| Package NDC: | 0378-3701-56 |
| Package Description: | 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0378-3701-56) |
NDC Information of Rizatriptan Benzoate
| NDC Code | 0378-3701-56 |
| Proprietary Name | Rizatriptan Benzoate |
| Package Description | 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (0378-3701-56) |
| Product NDC | 0378-3701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rizatriptan benzoate |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20121231 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| 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] |
