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Sumatriptan Succinate - 59115-078-99 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 59115-078
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan Succinate

Product NDC: 59115-078
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078298
Marketing Category: ANDA
Start Marketing Date: 20090907

Package Information of Sumatriptan Succinate

Package NDC: 59115-078-99
Package Description: 1 TABLET, FILM COATED in 1 DRUM (59115-078-99)

NDC Information of Sumatriptan Succinate

NDC Code 59115-078-99
Proprietary Name Sumatriptan Succinate
Package Description 1 TABLET, FILM COATED in 1 DRUM (59115-078-99)
Product NDC 59115-078
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090907
Marketing Category Name ANDA
Labeler Name Hikma Pharmaceutical
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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