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Axert
Axert - 0062-2080-06 - (almotriptan malate)
Drug Information of Axert
| Product NDC: | 0062-2080 |
| Proprietary Name: | Axert |
| Non Proprietary Name: | almotriptan malate |
| Active Ingredient(s): | 6.25 mg/1 & nbsp; almotriptan malate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Axert
| Product NDC: | 0062-2080 |
| Labeler Name: | Ortho-McNeil-Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021001 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010507 |
Package Information of Axert
| Package NDC: | 0062-2080-06 |
| Package Description: | 6 TABLET, COATED in 1 BLISTER PACK (0062-2080-06) |
NDC Information of Axert
| NDC Code | 0062-2080-06 |
| Proprietary Name | Axert |
| Package Description | 6 TABLET, COATED in 1 BLISTER PACK (0062-2080-06) |
| Product NDC | 0062-2080 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | almotriptan malate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20010507 |
| Marketing Category Name | NDA |
| Labeler Name | Ortho-McNeil-Janssen Pharmaceuticals, Inc. |
| Substance Name | ALMOTRIPTAN MALATE |
| Strength Number | 6.25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
