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leader ibuprofen - 37205-350-85 - (Ibuprofen)

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Drug Information of leader ibuprofen

Product NDC: 37205-350
Proprietary Name: leader ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of leader ibuprofen

Product NDC: 37205-350
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 19900515

Package Information of leader ibuprofen

Package NDC: 37205-350-85
Package Description: 250 TABLET, FILM COATED in 1 BOTTLE (37205-350-85)

NDC Information of leader ibuprofen

NDC Code 37205-350-85
Proprietary Name leader ibuprofen
Package Description 250 TABLET, FILM COATED in 1 BOTTLE (37205-350-85)
Product NDC 37205-350
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19900515
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of leader ibuprofen


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