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Sumatriptan - 16714-533-11 - (Sumatriptan)

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Drug Information of Sumatriptan

Product NDC: 16714-533
Proprietary Name: Sumatriptan
Non Proprietary Name: Sumatriptan
Active Ingredient(s): 100    mg/1 & nbsp;   Sumatriptan
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan

Product NDC: 16714-533
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078284
Marketing Category: ANDA
Start Marketing Date: 20110103

Package Information of Sumatriptan

Package NDC: 16714-533-11
Package Description: 1 BLISTER PACK in 1 CARTON (16714-533-11) > 9 TABLET, FILM COATED in 1 BLISTER PACK (16714-533-10)

NDC Information of Sumatriptan

NDC Code 16714-533-11
Proprietary Name Sumatriptan
Package Description 1 BLISTER PACK in 1 CARTON (16714-533-11) > 9 TABLET, FILM COATED in 1 BLISTER PACK (16714-533-10)
Product NDC 16714-533
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110103
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 100
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 Sumatriptan


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