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Sumatriptan Succinate - 0378-5630-01 - (sumatriptan succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 0378-5630
Proprietary Name: Sumatriptan Succinate
Non Proprietary Name: sumatriptan succinate
Active Ingredient(s): 25    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: 0378-5630
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077744
Marketing Category: ANDA
Start Marketing Date: 20130118

Package Information of Sumatriptan Succinate

Package NDC: 0378-5630-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5630-01)

NDC Information of Sumatriptan Succinate

NDC Code 0378-5630-01
Proprietary Name Sumatriptan Succinate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5630-01)
Product NDC 0378-5630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130118
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 25
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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