ibuprofen - 56062-255-10 - (Ibuprofen)

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Drug Information of ibuprofen

Product NDC: 56062-255
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 50    mg/1.25mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 56062-255
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075217
Marketing Category: ANDA
Start Marketing Date: 20110909

Package Information of ibuprofen

Package NDC: 56062-255-10
Package Description: 1 BOTTLE in 1 CARTON (56062-255-10) > 30 mL in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 56062-255-10
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (56062-255-10) > 30 mL in 1 BOTTLE
Product NDC 56062-255
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 20110909
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name IBUPROFEN
Strength Number 50
Strength Unit mg/1.25mL
Pharmaceutical Classes

Complete Information of ibuprofen


General Information