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zolmiptriptan - 68462-500-33 - (zolmitriptan)

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Drug Information of zolmiptriptan

Product NDC: 68462-500
Proprietary Name: zolmiptriptan
Non Proprietary Name: zolmitriptan
Active Ingredient(s): 5    mg/1 & nbsp;   zolmitriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of zolmiptriptan

Product NDC: 68462-500
Labeler Name: Glenmark Generics Inc.,USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202560
Marketing Category: ANDA
Start Marketing Date: 20130514

Package Information of zolmiptriptan

Package NDC: 68462-500-33
Package Description: 1 BLISTER PACK in 1 CARTON (68462-500-33) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of zolmiptriptan

NDC Code 68462-500-33
Proprietary Name zolmiptriptan
Package Description 1 BLISTER PACK in 1 CARTON (68462-500-33) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 68462-500
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolmitriptan
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130514
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc.,USA
Substance Name ZOLMITRIPTAN
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]

Complete Information of zolmiptriptan


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