Ibuprofen - 49999-097-28 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 49999-097
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 400    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 49999-097
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078558
Marketing Category: ANDA
Start Marketing Date: 20111121

Package Information of Ibuprofen

Package NDC: 49999-097-28
Package Description: 28 TABLET in 1 BOTTLE (49999-097-28)

NDC Information of Ibuprofen

NDC Code 49999-097-28
Proprietary Name Ibuprofen
Package Description 28 TABLET in 1 BOTTLE (49999-097-28)
Product NDC 49999-097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111121
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name IBUPROFEN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ibuprofen


General Information