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SUMATRIPTAN SUCCINATE - 0781-3169-07 - (sumatriptan succinate)

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Drug Information of SUMATRIPTAN SUCCINATE

Product NDC: 0781-3169
Proprietary Name: SUMATRIPTAN SUCCINATE
Non Proprietary Name: sumatriptan succinate
Active Ingredient(s): 4    mg/.5mL & nbsp;   sumatriptan succinate
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SUMATRIPTAN SUCCINATE

Product NDC: 0781-3169
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020080
Marketing Category: NDA
Start Marketing Date: 20120112

Package Information of SUMATRIPTAN SUCCINATE

Package NDC: 0781-3169-07
Package Description: 1 PACKAGE in 1 CARTON (0781-3169-07) > 2 SYRINGE in 1 PACKAGE > .5 mL in 1 SYRINGE

NDC Information of SUMATRIPTAN SUCCINATE

NDC Code 0781-3169-07
Proprietary Name SUMATRIPTAN SUCCINATE
Package Description 1 PACKAGE in 1 CARTON (0781-3169-07) > 2 SYRINGE in 1 PACKAGE > .5 mL in 1 SYRINGE
Product NDC 0781-3169
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20120112
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 4
Strength Unit mg/.5mL
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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