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Zolmitriptan Orally Disintegrating - 0115-0691-51 - (Zolmitriptan)

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Drug Information of Zolmitriptan Orally Disintegrating

Product NDC: 0115-0691
Proprietary Name: Zolmitriptan Orally Disintegrating
Non Proprietary Name: Zolmitriptan
Active Ingredient(s): 2.5    mg/1 & nbsp;   Zolmitriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Zolmitriptan Orally Disintegrating

Product NDC: 0115-0691
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021231
Marketing Category: NDA
Start Marketing Date: 20130514

Package Information of Zolmitriptan Orally Disintegrating

Package NDC: 0115-0691-51
Package Description: 1 BLISTER PACK in 1 CARTON (0115-0691-51) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Zolmitriptan Orally Disintegrating

NDC Code 0115-0691-51
Proprietary Name Zolmitriptan Orally Disintegrating
Package Description 1 BLISTER PACK in 1 CARTON (0115-0691-51) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 0115-0691
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 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 Orally Disintegrating


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