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Zolmitriptan - 68382-717-82 - (Zolmitriptan)

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Drug Information of Zolmitriptan

Product NDC: 68382-717
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: 68382-717
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202890
Marketing Category: ANDA
Start Marketing Date: 20130516

Package Information of Zolmitriptan

Package NDC: 68382-717-82
Package Description: 1 BLISTER PACK in 1 CARTON (68382-717-82) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-717-87)

NDC Information of Zolmitriptan

NDC Code 68382-717-82
Proprietary Name Zolmitriptan
Package Description 1 BLISTER PACK in 1 CARTON (68382-717-82) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-717-87)
Product NDC 68382-717
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolmitriptan
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130516
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) 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 Zolmitriptan


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