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Equaline ibuprofen - 41163-166-26 - (Ibuprofen)

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Drug Information of Equaline ibuprofen

Product NDC: 41163-166
Proprietary Name: Equaline 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 Equaline ibuprofen

Product NDC: 41163-166
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 20041007

Package Information of Equaline ibuprofen

Package NDC: 41163-166-26
Package Description: 1 BOTTLE in 1 CARTON (41163-166-26) > 120 mL in 1 BOTTLE

NDC Information of Equaline ibuprofen

NDC Code 41163-166-26
Proprietary Name Equaline ibuprofen
Package Description 1 BOTTLE in 1 CARTON (41163-166-26) > 120 mL in 1 BOTTLE
Product NDC 41163-166
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20041007
Marketing Category Name ANDA
Labeler Name Supervalu Inc
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Equaline ibuprofen


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