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Sumatriptan Succinate - 21695-874-09 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 21695-874
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
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan Succinate

Product NDC: 21695-874
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076847
Marketing Category: ANDA
Start Marketing Date: 20091117

Package Information of Sumatriptan Succinate

Package NDC: 21695-874-09
Package Description: 9 BLISTER PACK in 1 CARTON (21695-874-09) > 9 TABLET in 1 BLISTER PACK

NDC Information of Sumatriptan Succinate

NDC Code 21695-874-09
Proprietary Name Sumatriptan Succinate
Package Description 9 BLISTER PACK in 1 CARTON (21695-874-09) > 9 TABLET in 1 BLISTER PACK
Product NDC 21695-874
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091117
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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