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Sumatriptan Succinate - 16590-300-09 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 16590-300
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: 16590-300
Labeler Name: Stat Rx USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020132
Marketing Category: NDA
Start Marketing Date: 20080701

Package Information of Sumatriptan Succinate

Package NDC: 16590-300-09
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK (16590-300-09)

NDC Information of Sumatriptan Succinate

NDC Code 16590-300-09
Proprietary Name Sumatriptan Succinate
Package Description 9 TABLET, FILM COATED in 1 BLISTER PACK (16590-300-09)
Product NDC 16590-300
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080701
Marketing Category Name NDA
Labeler Name Stat Rx USA
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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