KETOPROFEN - 16590-136-90 - (KETOPROFEN)

Alphabetical Index


Drug Information of KETOPROFEN

Product NDC: 16590-136
Proprietary Name: KETOPROFEN
Non Proprietary Name: KETOPROFEN
Active Ingredient(s): 50    mg/1 & nbsp;   KETOPROFEN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of KETOPROFEN

Product NDC: 16590-136
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073516
Marketing Category: ANDA
Start Marketing Date: 20110118

Package Information of KETOPROFEN

Package NDC: 16590-136-90
Package Description: 90 CAPSULE in 1 BOTTLE (16590-136-90)

NDC Information of KETOPROFEN

NDC Code 16590-136-90
Proprietary Name KETOPROFEN
Package Description 90 CAPSULE in 1 BOTTLE (16590-136-90)
Product NDC 16590-136
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 STAT RX USA LLC
Substance Name KETOPROFEN
Strength Number 50
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