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Zolmitriptan - 60505-3719-0 - (Zolmitriptan)

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Drug Information of Zolmitriptan

Product NDC: 60505-3719
Proprietary Name: Zolmitriptan
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 Zolmitriptan

Product NDC: 60505-3719
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202476
Marketing Category: ANDA
Start Marketing Date: 20130514

Package Information of Zolmitriptan

Package NDC: 60505-3719-0
Package Description: 1 BLISTER PACK in 1 CARTON (60505-3719-0) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Zolmitriptan

NDC Code 60505-3719-0
Proprietary Name Zolmitriptan
Package Description 1 BLISTER PACK in 1 CARTON (60505-3719-0) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 60505-3719
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 Apotex Corp
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 Zolmitriptan


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