IMITREX - 54868-3180-0 - (sumatriptan succinate)

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Drug Information of IMITREX

Product NDC: 54868-3180
Proprietary Name: IMITREX
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 IMITREX

Product NDC: 54868-3180
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020080
Marketing Category: NDA
Start Marketing Date: 19950126

Package Information of IMITREX

Package NDC: 54868-3180-0
Package Description: 2 SYRINGE in 1 PACKAGE (54868-3180-0) > .5 mL in 1 SYRINGE

NDC Information of IMITREX

NDC Code 54868-3180-0
Proprietary Name IMITREX
Package Description 2 SYRINGE in 1 PACKAGE (54868-3180-0) > .5 mL in 1 SYRINGE
Product NDC 54868-3180
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 19950126
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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 IMITREX


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