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Sumatriptan Succinate - 0093-0222-90 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 0093-0222
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: 0093-0222
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076840
Marketing Category: ANDA
Start Marketing Date: 20090209

Package Information of Sumatriptan Succinate

Package NDC: 0093-0222-90
Package Description: 9 BLISTER PACK in 1 BOX (0093-0222-90) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-0222-19)

NDC Information of Sumatriptan Succinate

NDC Code 0093-0222-90
Proprietary Name Sumatriptan Succinate
Package Description 9 BLISTER PACK in 1 BOX (0093-0222-90) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-0222-19)
Product NDC 0093-0222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090209
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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