AXERT - 50458-210-01 - (almotriptan malate)

Alphabetical Index


Drug Information of AXERT

Product NDC: 50458-210
Proprietary Name: AXERT
Non Proprietary Name: almotriptan malate
Active Ingredient(s): 12.5    mg/1 & nbsp;   almotriptan malate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of AXERT

Product NDC: 50458-210
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021001
Marketing Category: NDA
Start Marketing Date: 20010507

Package Information of AXERT

Package NDC: 50458-210-01
Package Description: 12 TABLET, COATED in 1 BLISTER PACK (50458-210-01)

NDC Information of AXERT

NDC Code 50458-210-01
Proprietary Name AXERT
Package Description 12 TABLET, COATED in 1 BLISTER PACK (50458-210-01)
Product NDC 50458-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name almotriptan malate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20010507
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name ALMOTRIPTAN MALATE
Strength Number 12.5
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 AXERT


General Information