Product NDC: | 68462-497 |
Proprietary Name: | Zolmitriptan |
Non Proprietary Name: | Zolmitriptan |
Active Ingredient(s): | 2.5 mg/1 & nbsp; Zolmitriptan |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68462-497 |
Labeler Name: | Glenmark Generics Inc.,USA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA201779 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130514 |
Package NDC: | 68462-497-76 |
Package Description: | 1 BLISTER PACK in 1 CARTON (68462-497-76) > 6 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 68462-497-76 |
Proprietary Name | Zolmitriptan |
Package Description | 1 BLISTER PACK in 1 CARTON (68462-497-76) > 6 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 68462-497 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Zolmitriptan |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130514 |
Marketing Category Name | ANDA |
Labeler Name | Glenmark Generics Inc.,USA |
Substance Name | ZOLMITRIPTAN |
Strength Number | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |