IBUPROFEN - 0363-0003-40 - (ibuprofen)

Alphabetical Index


Drug Information of IBUPROFEN

Product NDC: 0363-0003
Proprietary Name: IBUPROFEN
Non Proprietary Name: ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   ibuprofen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of IBUPROFEN

Product NDC: 0363-0003
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079205
Marketing Category: ANDA
Start Marketing Date: 20110509

Package Information of IBUPROFEN

Package NDC: 0363-0003-40
Package Description: 1 BOTTLE in 1 CARTON (0363-0003-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Information of IBUPROFEN

NDC Code 0363-0003-40
Proprietary Name IBUPROFEN
Package Description 1 BOTTLE in 1 CARTON (0363-0003-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product NDC 0363-0003
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20110509
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IBUPROFEN


General Information