Ibuprofen - 43063-013-06 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 43063-013
Proprietary Name: Ibuprofen
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 Ibuprofen

Product NDC: 43063-013
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078558
Marketing Category: ANDA
Start Marketing Date: 20091123

Package Information of Ibuprofen

Package NDC: 43063-013-06
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC (43063-013-06)

NDC Information of Ibuprofen

NDC Code 43063-013-06
Proprietary Name Ibuprofen
Package Description 6 TABLET in 1 BOTTLE, PLASTIC (43063-013-06)
Product NDC 43063-013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091123
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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 Ibuprofen


General Information