ibuprofen - 41250-660-26 - (Ibuprofen)

Alphabetical Index


Drug Information of ibuprofen

Product NDC: 41250-660
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 41250-660
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 20020319

Package Information of ibuprofen

Package NDC: 41250-660-26
Package Description: 1 BOTTLE in 1 CARTON (41250-660-26) > 120 mL in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 41250-660-26
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (41250-660-26) > 120 mL in 1 BOTTLE
Product NDC 41250-660
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20020319
Marketing Category Name ANDA
Labeler Name Meijer Distribution Inc
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of ibuprofen


General Information