Home > National Drug Code (NDC) > Leflunomide

Leflunomide - 0093-0173-56 - (Leflunomide)

Alphabetical Index


Drug Information of Leflunomide

Product NDC: 0093-0173
Proprietary Name: Leflunomide
Non Proprietary Name: Leflunomide
Active Ingredient(s): 10    mg/1 & nbsp;   Leflunomide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Leflunomide

Product NDC: 0093-0173
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077084
Marketing Category: ANDA
Start Marketing Date: 20050914

Package Information of Leflunomide

Package NDC: 0093-0173-56
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-0173-56)

NDC Information of Leflunomide

NDC Code 0093-0173-56
Proprietary Name Leflunomide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0093-0173-56)
Product NDC 0093-0173
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Leflunomide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050914
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name LEFLUNOMIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Leflunomide


General Information