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Leflunomide - 54868-2319-0 - (leflunomide)

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Drug Information of Leflunomide

Product NDC: 54868-2319
Proprietary Name: Leflunomide
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 Leflunomide

Product NDC: 54868-2319
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077087
Marketing Category: ANDA
Start Marketing Date: 20060710

Package Information of Leflunomide

Package NDC: 54868-2319-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-2319-0)

NDC Information of Leflunomide

NDC Code 54868-2319-0
Proprietary Name Leflunomide
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-2319-0)
Product NDC 54868-2319
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name leflunomide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060710
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LEFLUNOMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Leflunomide


General Information