Ibuprofen - 57910-403-22 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 57910-403
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 57910-403
Labeler Name: Shasun Pharmaceuticals Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079129
Marketing Category: ANDA
Start Marketing Date: 20110328

Package Information of Ibuprofen

Package NDC: 57910-403-22
Package Description: 1 BOTTLE in 1 CARTON (57910-403-22) > 24 TABLET, COATED in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 57910-403-22
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (57910-403-22) > 24 TABLET, COATED in 1 BOTTLE
Product NDC 57910-403
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20110328
Marketing Category Name ANDA
Labeler Name Shasun Pharmaceuticals Limited
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information