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LEFLUNOMIDE - 60505-2502-2 - (LEFLUNOMIDE)

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Drug Information of LEFLUNOMIDE

Product NDC: 60505-2502
Proprietary Name: LEFLUNOMIDE
Non Proprietary Name: LEFLUNOMIDE
Active Ingredient(s): 10    mg/1 & nbsp;   LEFLUNOMIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEFLUNOMIDE

Product NDC: 60505-2502
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077090
Marketing Category: ANDA
Start Marketing Date: 20050913

Package Information of LEFLUNOMIDE

Package NDC: 60505-2502-2
Package Description: 100 TABLET in 1 BOTTLE (60505-2502-2)

NDC Information of LEFLUNOMIDE

NDC Code 60505-2502-2
Proprietary Name LEFLUNOMIDE
Package Description 100 TABLET in 1 BOTTLE (60505-2502-2)
Product NDC 60505-2502
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEFLUNOMIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050913
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name LEFLUNOMIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of LEFLUNOMIDE


General Information