Ibuprofen - 57344-109-03 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 57344-109
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: 57344-109
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079129
Marketing Category: ANDA
Start Marketing Date: 20121204

Package Information of Ibuprofen

Package NDC: 57344-109-03
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (57344-109-03) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 57344-109-03
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (57344-109-03) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 57344-109
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121204
Marketing Category Name ANDA
Labeler Name AAA Pharmaceutical, Inc.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information