Ibuprofen - 0363-0413-27 - (Diphenhydramine citrate, Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 0363-0413
Proprietary Name: Ibuprofen
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

Product NDC: 0363-0413
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079113
Marketing Category: ANDA
Start Marketing Date: 20100209

Package Information of Ibuprofen

Package NDC: 0363-0413-27
Package Description: 1 BOTTLE in 1 CARTON (0363-0413-27) > 80 TABLET, COATED in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 0363-0413-27
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (0363-0413-27) > 80 TABLET, COATED in 1 BOTTLE
Product NDC 0363-0413
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine citrate, Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20100209
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information