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sumatriptan succinate - 42023-121-05 - (sumatriptan succinate)

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Drug Information of sumatriptan succinate

Product NDC: 42023-121
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: 42023-121
Labeler Name: JHP Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077871
Marketing Category: ANDA
Start Marketing Date: 20090806

Package Information of sumatriptan succinate

Package NDC: 42023-121-05
Package Description: 5 VIAL in 1 CARTON (42023-121-05) > .5 mL in 1 VIAL (42023-121-01)

NDC Information of sumatriptan succinate

NDC Code 42023-121-05
Proprietary Name sumatriptan succinate
Package Description 5 VIAL in 1 CARTON (42023-121-05) > .5 mL in 1 VIAL (42023-121-01)
Product NDC 42023-121
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20090806
Marketing Category Name ANDA
Labeler Name JHP Pharmaceuticals 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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