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Leader Ibuprofen - 37205-282-26 - (Ibuprofen)

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Drug Information of Leader Ibuprofen

Product NDC: 37205-282
Proprietary Name: Leader Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Leader Ibuprofen

Product NDC: 37205-282
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 20020508

Package Information of Leader Ibuprofen

Package NDC: 37205-282-26
Package Description: 1 BOTTLE in 1 CARTON (37205-282-26) > 120 mL in 1 BOTTLE

NDC Information of Leader Ibuprofen

NDC Code 37205-282-26
Proprietary Name Leader Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (37205-282-26) > 120 mL in 1 BOTTLE
Product NDC 37205-282
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20020508
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Leader Ibuprofen


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