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good sense ibuprofen pm - 0113-0050-58 - (diphenhydramine citrate, ibuprofen)

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Drug Information of good sense ibuprofen pm

Product NDC: 0113-0050
Proprietary Name: good sense 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 good sense ibuprofen pm

Product NDC: 0113-0050
Labeler Name: L Perrigo Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079113
Marketing Category: ANDA
Start Marketing Date: 20090305

Package Information of good sense ibuprofen pm

Package NDC: 0113-0050-58
Package Description: 1 BOTTLE in 1 CARTON (0113-0050-58) > 40 TABLET, COATED in 1 BOTTLE

NDC Information of good sense ibuprofen pm

NDC Code 0113-0050-58
Proprietary Name good sense ibuprofen pm
Package Description 1 BOTTLE in 1 CARTON (0113-0050-58) > 40 TABLET, COATED in 1 BOTTLE
Product NDC 0113-0050
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine citrate, ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090305
Marketing Category Name ANDA
Labeler Name L Perrigo Company
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of good sense ibuprofen pm


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