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Sumatriptan - 65862-147-36 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan

Product NDC: 65862-147
Proprietary Name: Sumatriptan
Non Proprietary Name: Sumatriptan Succinate
Active Ingredient(s): 50    mg/1 & nbsp;   Sumatriptan Succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan

Product NDC: 65862-147
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078327
Marketing Category: ANDA
Start Marketing Date: 20090817

Package Information of Sumatriptan

Package NDC: 65862-147-36
Package Description: 1 BLISTER PACK in 1 CARTON (65862-147-36) > 9 TABLET in 1 BLISTER PACK

NDC Information of Sumatriptan

NDC Code 65862-147-36
Proprietary Name Sumatriptan
Package Description 1 BLISTER PACK in 1 CARTON (65862-147-36) > 9 TABLET in 1 BLISTER PACK
Product NDC 65862-147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090817
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 50
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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