IBU - 49999-042-00 - (Ibuprofen)

Alphabetical Index


Drug Information of IBU

Product NDC: 49999-042
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: 49999-042
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076112
Marketing Category: ANDA
Start Marketing Date: 20101019

Package Information of IBU

Package NDC: 49999-042-00
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (49999-042-00)

NDC Information of IBU

NDC Code 49999-042-00
Proprietary Name IBU
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (49999-042-00)
Product NDC 49999-042
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101019
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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