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ibuprofen ib - 42507-074-78 - (Ibuprofen)

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Drug Information of ibuprofen ib

Product NDC: 42507-074
Proprietary Name: ibuprofen ib
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen ib

Product NDC: 42507-074
Labeler Name: HyVee Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077349
Marketing Category: ANDA
Start Marketing Date: 20060514

Package Information of ibuprofen ib

Package NDC: 42507-074-78
Package Description: 1 BOTTLE in 1 CARTON (42507-074-78) > 100 TABLET, COATED in 1 BOTTLE

NDC Information of ibuprofen ib

NDC Code 42507-074-78
Proprietary Name ibuprofen ib
Package Description 1 BOTTLE in 1 CARTON (42507-074-78) > 100 TABLET, COATED in 1 BOTTLE
Product NDC 42507-074
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20060514
Marketing Category Name ANDA
Labeler Name HyVee Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen ib


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