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ibuprofen pm - 56062-050-58 - (diphenhydramine citrate, ibuprofen)

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Drug Information of ibuprofen pm

Product NDC: 56062-050
Proprietary Name: ibuprofen pm
Non Proprietary Name: diphenhydramine citrate, ibuprofen
Active Ingredient(s): 38; 200    mg/1; mg/1 & nbsp;   diphenhydramine citrate, ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen pm

Product NDC: 56062-050
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079113
Marketing Category: ANDA
Start Marketing Date: 20110915

Package Information of ibuprofen pm

Package NDC: 56062-050-58
Package Description: 1 BOTTLE in 1 CARTON (56062-050-58) > 40 TABLET, COATED in 1 BOTTLE

NDC Information of ibuprofen pm

NDC Code 56062-050-58
Proprietary Name ibuprofen pm
Package Description 1 BOTTLE in 1 CARTON (56062-050-58) > 40 TABLET, COATED in 1 BOTTLE
Product NDC 56062-050
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine citrate, ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20110915
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ibuprofen pm


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