Ketoprofen - 55289-181-20 - (Ketoprofen)

Alphabetical Index


Drug Information of Ketoprofen

Product NDC: 55289-181
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: 55289-181
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073517
Marketing Category: ANDA
Start Marketing Date: 20110118

Package Information of Ketoprofen

Package NDC: 55289-181-20
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-181-20)

NDC Information of Ketoprofen

NDC Code 55289-181-20
Proprietary Name Ketoprofen
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (55289-181-20)
Product NDC 55289-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoprofen
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110118
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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