IBU - 55111-684-30 - (Ibuprofen)

Alphabetical Index


Drug Information of IBU

Product NDC: 55111-684
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: 55111-684
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20081120

Package Information of IBU

Package NDC: 55111-684-30
Package Description: 30 TABLET in 1 BOTTLE (55111-684-30)

NDC Information of IBU

NDC Code 55111-684-30
Proprietary Name IBU
Package Description 30 TABLET in 1 BOTTLE (55111-684-30)
Product NDC 55111-684
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081120
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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