ibuprofen - 56062-461-62 - (Ibuprofen)

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Drug Information of ibuprofen

Product NDC: 56062-461
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 56062-461
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076359
Marketing Category: ANDA
Start Marketing Date: 20041028

Package Information of ibuprofen

Package NDC: 56062-461-62
Package Description: 1 BOTTLE in 1 CARTON (56062-461-62) > 24 TABLET, CHEWABLE in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 56062-461-62
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (56062-461-62) > 24 TABLET, CHEWABLE in 1 BOTTLE
Product NDC 56062-461
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20041028
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information