MAXALT - 54868-4251-1 - (rizatriptan benzoate)

Alphabetical Index


Drug Information of MAXALT

Product NDC: 54868-4251
Proprietary Name: MAXALT
Non Proprietary Name: rizatriptan benzoate
Active Ingredient(s): 10    mg/1 & nbsp;   rizatriptan benzoate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of MAXALT

Product NDC: 54868-4251
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020864
Marketing Category: NDA
Start Marketing Date: 20070824

Package Information of MAXALT

Package NDC: 54868-4251-1
Package Description: 3 TABLET in 1 BOTTLE (54868-4251-1)

NDC Information of MAXALT

NDC Code 54868-4251-1
Proprietary Name MAXALT
Package Description 3 TABLET in 1 BOTTLE (54868-4251-1)
Product NDC 54868-4251
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rizatriptan benzoate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070824
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name RIZATRIPTAN BENZOATE
Strength Number 10
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 MAXALT


General Information