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Zolmitriptan - 0115-0671-51 - (Zolmitriptan)

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Drug Information of Zolmitriptan

Product NDC: 0115-0671
Proprietary Name: Zolmitriptan
Non Proprietary Name: Zolmitriptan
Active Ingredient(s): 2.5    mg/1 & nbsp;   Zolmitriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zolmitriptan

Product NDC: 0115-0671
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020768
Marketing Category: NDA
Start Marketing Date: 20130514

Package Information of Zolmitriptan

Package NDC: 0115-0671-51
Package Description: 1 BLISTER PACK in 1 CARTON (0115-0671-51) > 6 TABLET in 1 BLISTER PACK

NDC Information of Zolmitriptan

NDC Code 0115-0671-51
Proprietary Name Zolmitriptan
Package Description 1 BLISTER PACK in 1 CARTON (0115-0671-51) > 6 TABLET in 1 BLISTER PACK
Product NDC 0115-0671
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolmitriptan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130514
Marketing Category Name NDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
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


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