Ketoprofen - 54868-2415-2 - (ketoprofen)

Alphabetical Index


Drug Information of Ketoprofen

Product NDC: 54868-2415
Proprietary Name: Ketoprofen
Non Proprietary Name: ketoprofen
Active Ingredient(s): 75    mg/1 & nbsp;   ketoprofen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Ketoprofen

Product NDC: 54868-2415
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074035
Marketing Category: ANDA
Start Marketing Date: 20050815

Package Information of Ketoprofen

Package NDC: 54868-2415-2
Package Description: 30 CAPSULE in 1 BOTTLE (54868-2415-2)

NDC Information of Ketoprofen

NDC Code 54868-2415-2
Proprietary Name Ketoprofen
Package Description 30 CAPSULE in 1 BOTTLE (54868-2415-2)
Product NDC 54868-2415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketoprofen
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050815
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name KETOPROFEN
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ketoprofen


General Information