Ketoprofen - 0093-3195-01 - (Ketoprofen)

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Drug Information of Ketoprofen

Product NDC: 0093-3195
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: 0093-3195
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073517
Marketing Category: ANDA
Start Marketing Date: 19930101

Package Information of Ketoprofen

Package NDC: 0093-3195-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-3195-01)

NDC Information of Ketoprofen

NDC Code 0093-3195-01
Proprietary Name Ketoprofen
Package Description 100 CAPSULE in 1 BOTTLE (0093-3195-01)
Product NDC 0093-3195
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketoprofen
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19930101
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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