Ibuprofen - 53808-0271-1 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 53808-0271
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: 53808-0271
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078558
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Ibuprofen

Package NDC: 53808-0271-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0271-1)

NDC Information of Ibuprofen

NDC Code 53808-0271-1
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BLISTER PACK (53808-0271-1)
Product NDC 53808-0271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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