Ibuprofen - 57896-941-25 - (ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 57896-941
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: 57896-941
Labeler Name: Geri-Care Pharmaceutical Corp
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 20040101

Package Information of Ibuprofen

Package NDC: 57896-941-25
Package Description: 250 TABLET, FILM COATED in 1 BOTTLE (57896-941-25)

NDC Information of Ibuprofen

NDC Code 57896-941-25
Proprietary Name Ibuprofen
Package Description 250 TABLET, FILM COATED in 1 BOTTLE (57896-941-25)
Product NDC 57896-941
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040101
Marketing Category Name ANDA
Labeler Name Geri-Care Pharmaceutical Corp
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information