Ketoprofen - 0378-8200-01 - (ketoprofen)

Alphabetical Index


Drug Information of Ketoprofen

Product NDC: 0378-8200
Proprietary Name: Ketoprofen
Non Proprietary Name: ketoprofen
Active Ingredient(s): 200    mg/1 & nbsp;   ketoprofen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Ketoprofen

Product NDC: 0378-8200
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075679
Marketing Category: ANDA
Start Marketing Date: 20120119

Package Information of Ketoprofen

Package NDC: 0378-8200-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0378-8200-01)

NDC Information of Ketoprofen

NDC Code 0378-8200-01
Proprietary Name Ketoprofen
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0378-8200-01)
Product NDC 0378-8200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketoprofen
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120119
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name KETOPROFEN
Strength Number 200
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