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AXERT
AXERT - 50458-211-01 - (almotriptan malate)
Drug Information of AXERT
| Product NDC: | 50458-211 |
| 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: | 50458-211 |
| Labeler Name: | 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: | 50458-211-01 |
| Package Description: | 6 TABLET, COATED in 1 BLISTER PACK (50458-211-01) |
NDC Information of AXERT
| NDC Code | 50458-211-01 |
| Proprietary Name | AXERT |
| Package Description | 6 TABLET, COATED in 1 BLISTER PACK (50458-211-01) |
| Product NDC | 50458-211 |
| 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 | 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] |
