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Sumatriptan - 59762-1851-9 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan

Product NDC: 59762-1851
Proprietary Name: Sumatriptan
Non Proprietary Name: Sumatriptan Succinate
Active Ingredient(s): 50    mg/1 & nbsp;   Sumatriptan Succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan

Product NDC: 59762-1851
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078327
Marketing Category: ANDA
Start Marketing Date: 20090817

Package Information of Sumatriptan

Package NDC: 59762-1851-9
Package Description: 1 BLISTER PACK in 1 CARTON (59762-1851-9) > 9 TABLET in 1 BLISTER PACK (59762-1851-3)

NDC Information of Sumatriptan

NDC Code 59762-1851-9
Proprietary Name Sumatriptan
Package Description 1 BLISTER PACK in 1 CARTON (59762-1851-9) > 9 TABLET in 1 BLISTER PACK (59762-1851-3)
Product NDC 59762-1851
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090817
Marketing Category Name ANDA
Labeler Name Greenstone LLC
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


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