IMITREX - 54868-5118-0 - (sumatriptan succinate)

Alphabetical Index


Drug Information of IMITREX

Product NDC: 54868-5118
Proprietary Name: IMITREX
Non Proprietary Name: sumatriptan succinate
Active Ingredient(s): 100    mg/1 & nbsp;   sumatriptan succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of IMITREX

Product NDC: 54868-5118
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020132
Marketing Category: NDA
Start Marketing Date: 20040714

Package Information of IMITREX

Package NDC: 54868-5118-0
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK (54868-5118-0)

NDC Information of IMITREX

NDC Code 54868-5118-0
Proprietary Name IMITREX
Package Description 9 TABLET, FILM COATED in 1 BLISTER PACK (54868-5118-0)
Product NDC 54868-5118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sumatriptan succinate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040714
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name SUMATRIPTAN SUCCINATE
Strength Number 100
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 IMITREX


General Information