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Berkley and Jensen Ibuprofen - 68391-604-90 - (Ibuprofen)

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Drug Information of Berkley and Jensen Ibuprofen

Product NDC: 68391-604
Proprietary Name: Berkley and Jensen Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Berkley and Jensen Ibuprofen

Product NDC: 68391-604
Labeler Name: BJWC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 20070620

Package Information of Berkley and Jensen Ibuprofen

Package NDC: 68391-604-90
Package Description: 500 TABLET in 1 BOTTLE (68391-604-90)

NDC Information of Berkley and Jensen Ibuprofen

NDC Code 68391-604-90
Proprietary Name Berkley and Jensen Ibuprofen
Package Description 500 TABLET in 1 BOTTLE (68391-604-90)
Product NDC 68391-604
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070620
Marketing Category Name ANDA
Labeler Name BJWC
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Berkley and Jensen Ibuprofen


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