ibuprofen - 56062-647-71 - (Ibuprofen)

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Drug Information of ibuprofen

Product NDC: 56062-647
Proprietary Name: 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 ibuprofen

Product NDC: 56062-647
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 19880915

Package Information of ibuprofen

Package NDC: 56062-647-71
Package Description: 1 BOTTLE in 1 CARTON (56062-647-71) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 56062-647-71
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (56062-647-71) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 56062-647
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19880915
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information