Ibuprofen - 21695-067-30 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 21695-067
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 600    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 21695-067
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075682
Marketing Category: ANDA
Start Marketing Date: 20090610

Package Information of Ibuprofen

Package NDC: 21695-067-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-067-30)

NDC Information of Ibuprofen

NDC Code 21695-067-30
Proprietary Name Ibuprofen
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-067-30)
Product NDC 21695-067
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090610
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name IBUPROFEN
Strength Number 600
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