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Zolmitriptan - 68462-497-76 - (Zolmitriptan)

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Drug Information of Zolmitriptan

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)

Labeler Information of Zolmitriptan

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 Information of Zolmitriptan

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 Information of Zolmitriptan

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]

Complete Information of Zolmitriptan


General Information