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Leflunomide - 16714-331-04 - (leflunomide)

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Drug Information of Leflunomide

Product NDC: 16714-331
Proprietary Name: Leflunomide
Non Proprietary Name: leflunomide
Active Ingredient(s): 20    mg/1 & nbsp;   leflunomide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Leflunomide

Product NDC: 16714-331
Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091369
Marketing Category: ANDA
Start Marketing Date: 20110506

Package Information of Leflunomide

Package NDC: 16714-331-04
Package Description: 500 TABLET in 1 BOTTLE (16714-331-04)

NDC Information of Leflunomide

NDC Code 16714-331-04
Proprietary Name Leflunomide
Package Description 500 TABLET in 1 BOTTLE (16714-331-04)
Product NDC 16714-331
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name leflunomide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110506
Marketing Category Name ANDA
Labeler Name NorthStar RxLLC
Substance Name LEFLUNOMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Antirheumatic Agent [EPC]

Complete Information of Leflunomide


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