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SUMATRIPTAN SUCCINATE - 68258-3008-1 - (sumatriptan succinate)

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Drug Information of SUMATRIPTAN SUCCINATE

Product NDC: 68258-3008
Proprietary Name: SUMATRIPTAN SUCCINATE
Non Proprietary Name: sumatriptan succinate
Active Ingredient(s): 50    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: 68258-3008
Labeler Name: Dispensing Solutions Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020132
Marketing Category: NDA
Start Marketing Date: 20090303

Package Information of SUMATRIPTAN SUCCINATE

Package NDC: 68258-3008-1
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK (68258-3008-1)

NDC Information of SUMATRIPTAN SUCCINATE

NDC Code 68258-3008-1
Proprietary Name SUMATRIPTAN SUCCINATE
Package Description 9 TABLET, FILM COATED in 1 BLISTER PACK (68258-3008-1)
Product NDC 68258-3008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090303
Marketing Category Name NDA
Labeler Name Dispensing Solutions Inc.
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 SUCCINATE


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