IBU - 0179-0119-30 - (Ibuprofen)

Alphabetical Index


Drug Information of IBU

Product NDC: 0179-0119
Proprietary Name: IBU
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 800    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of IBU

Product NDC: 0179-0119
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20120605

Package Information of IBU

Package NDC: 0179-0119-30
Package Description: 30 TABLET in 1 BOTTLE (0179-0119-30)

NDC Information of IBU

NDC Code 0179-0119-30
Proprietary Name IBU
Package Description 30 TABLET in 1 BOTTLE (0179-0119-30)
Product NDC 0179-0119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120605
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name IBUPROFEN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of IBU


General Information