ibuprofen - 59779-604-59 - (Ibuprofen)

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Drug Information of ibuprofen

Product NDC: 59779-604
Proprietary Name: 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 ibuprofen

Product NDC: 59779-604
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 20010710

Package Information of ibuprofen

Package NDC: 59779-604-59
Package Description: 750 TABLET in 1 BOTTLE (59779-604-59)

NDC Information of ibuprofen

NDC Code 59779-604-59
Proprietary Name ibuprofen
Package Description 750 TABLET in 1 BOTTLE (59779-604-59)
Product NDC 59779-604
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010710
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information