ZOMIG ZMT - 64896-692-50 - (Zolmitriptan)

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Drug Information of ZOMIG ZMT

Product NDC: 64896-692
Proprietary Name: ZOMIG ZMT
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 ZOMIG ZMT

Product NDC: 64896-692
Labeler Name: Impax Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021231
Marketing Category: NDA
Start Marketing Date: 20120702

Package Information of ZOMIG ZMT

Package NDC: 64896-692-50
Package Description: 1 BLISTER PACK in 1 CARTON (64896-692-50) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of ZOMIG ZMT

NDC Code 64896-692-50
Proprietary Name ZOMIG ZMT
Package Description 1 BLISTER PACK in 1 CARTON (64896-692-50) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 64896-692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolmitriptan
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120702
Marketing Category Name NDA
Labeler Name Impax Laboratories, Inc.
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 ZOMIG ZMT


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