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Sumatriptan Succinate - 64679-728-01 - (Sumatriptan Succinate)

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Drug Information of Sumatriptan Succinate

Product NDC: 64679-728
Proprietary Name: Sumatriptan Succinate
Non Proprietary Name: Sumatriptan Succinate
Active Ingredient(s): 6    mg/.5mL & nbsp;   Sumatriptan Succinate
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sumatriptan Succinate

Product NDC: 64679-728
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078593
Marketing Category: ANDA
Start Marketing Date: 20090206

Package Information of Sumatriptan Succinate

Package NDC: 64679-728-01
Package Description: 5 VIAL in 1 CARTON (64679-728-01) > .5 mL in 1 VIAL

NDC Information of Sumatriptan Succinate

NDC Code 64679-728-01
Proprietary Name Sumatriptan Succinate
Package Description 5 VIAL in 1 CARTON (64679-728-01) > .5 mL in 1 VIAL
Product NDC 64679-728
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sumatriptan Succinate
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20090206
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 6
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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