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sumatriptan succinate - 62756-522-18 - (sumatriptan succinate)

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Drug Information of sumatriptan succinate

Product NDC: 62756-522
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: 62756-522
Labeler Name: SUN PHARMACEUTICAL INDUSTRIES LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078295
Marketing Category: ANDA
Start Marketing Date: 20090810

Package Information of sumatriptan succinate

Package NDC: 62756-522-18
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (62756-522-18)

NDC Information of sumatriptan succinate

NDC Code 62756-522-18
Proprietary Name sumatriptan succinate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (62756-522-18)
Product NDC 62756-522
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090810
Marketing Category Name ANDA
Labeler Name SUN PHARMACEUTICAL INDUSTRIES LIMITED
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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