Ibuprofen - 50844-291-08 - (ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 50844-291
Proprietary Name: Ibuprofen
Non Proprietary Name: ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 50844-291
Labeler Name: L.N.K. International, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 19990302

Package Information of Ibuprofen

Package NDC: 50844-291-08
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50844-291-08) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 50844-291-08
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50844-291-08) > 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 50844-291
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19990302
Marketing Category Name ANDA
Labeler Name L.N.K. International, Inc.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information