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Fenoprofen Calcium - 55289-334-30 - (Fenoprofen Calcium)

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Drug Information of Fenoprofen Calcium

Product NDC: 55289-334
Proprietary Name: Fenoprofen Calcium
Non Proprietary Name: Fenoprofen Calcium
Active Ingredient(s): 600    mg/1 & nbsp;   Fenoprofen Calcium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fenoprofen Calcium

Product NDC: 55289-334
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072267
Marketing Category: ANDA
Start Marketing Date: 20091123

Package Information of Fenoprofen Calcium

Package NDC: 55289-334-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-334-30)

NDC Information of Fenoprofen Calcium

NDC Code 55289-334-30
Proprietary Name Fenoprofen Calcium
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-334-30)
Product NDC 55289-334
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fenoprofen Calcium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091123
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name FENOPROFEN CALCIUM
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Fenoprofen Calcium


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