Ibuprofen - 16103-393-08 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 16103-393
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: 16103-393
Labeler Name: Pharbest Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079129
Marketing Category: ANDA
Start Marketing Date: 20110118

Package Information of Ibuprofen

Package NDC: 16103-393-08
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (16103-393-08) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 16103-393-08
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (16103-393-08) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 16103-393
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110118
Marketing Category Name ANDA
Labeler Name Pharbest Pharmaceuticals, Inc.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information