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Equaline ibuprofen - 41163-074-71 - (Ibuprofen)

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Drug Information of Equaline ibuprofen

Product NDC: 41163-074
Proprietary Name: Equaline ibuprofen
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 Equaline ibuprofen

Product NDC: 41163-074
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077349
Marketing Category: ANDA
Start Marketing Date: 20060307

Package Information of Equaline ibuprofen

Package NDC: 41163-074-71
Package Description: 1 BOTTLE in 1 CARTON (41163-074-71) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of Equaline ibuprofen

NDC Code 41163-074-71
Proprietary Name Equaline ibuprofen
Package Description 1 BOTTLE in 1 CARTON (41163-074-71) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 41163-074
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20060307
Marketing Category Name ANDA
Labeler Name Supervalu Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Equaline ibuprofen


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