Arava - 63629-1263-1 - (leflunomide)

Alphabetical Index


Drug Information of Arava

Product NDC: 63629-1263
Proprietary Name: Arava
Non Proprietary Name: leflunomide
Active Ingredient(s): 20    mg/1 & nbsp;   leflunomide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Arava

Product NDC: 63629-1263
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020905
Marketing Category: NDA
Start Marketing Date: 19980910

Package Information of Arava

Package NDC: 63629-1263-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-1263-1)

NDC Information of Arava

NDC Code 63629-1263-1
Proprietary Name Arava
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-1263-1)
Product NDC 63629-1263
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name leflunomide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980910
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name LEFLUNOMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Arava


General Information