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up and up ibuprofen pm - 11673-050-27 - (diphenhydramine citrate and ibuprofen)

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Drug Information of up and up ibuprofen pm

Product NDC: 11673-050
Proprietary Name: up and up ibuprofen pm
Non Proprietary Name: diphenhydramine citrate and ibuprofen
Active Ingredient(s): 38; 200    mg/1; mg/1 & nbsp;   diphenhydramine citrate and ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of up and up ibuprofen pm

Product NDC: 11673-050
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079113
Marketing Category: ANDA
Start Marketing Date: 20090710

Package Information of up and up ibuprofen pm

Package NDC: 11673-050-27
Package Description: 1 BOTTLE in 1 CARTON (11673-050-27) > 80 TABLET, COATED in 1 BOTTLE

NDC Information of up and up ibuprofen pm

NDC Code 11673-050-27
Proprietary Name up and up ibuprofen pm
Package Description 1 BOTTLE in 1 CARTON (11673-050-27) > 80 TABLET, COATED in 1 BOTTLE
Product NDC 11673-050
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine citrate and ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090710
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of up and up ibuprofen pm


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