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Sumatriptan Succinate - 52959-510-09 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 52959-510
Proprietary Name: Sumatriptan Succinate
Non Proprietary Name: Sumatriptan Succinate
Active Ingredient(s): 100    mg/1 & nbsp;   Sumatriptan Succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan Succinate

Product NDC: 52959-510
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076847
Marketing Category: ANDA
Start Marketing Date: 20091117

Package Information of Sumatriptan Succinate

Package NDC: 52959-510-09
Package Description: 9 TABLET in 1 BOTTLE (52959-510-09)

NDC Information of Sumatriptan Succinate

NDC Code 52959-510-09
Proprietary Name Sumatriptan Succinate
Package Description 9 TABLET in 1 BOTTLE (52959-510-09)
Product NDC 52959-510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091117
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
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 Succinate


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