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FENOFIBRATE - 60760-900-30 - (FENOFIBRATE)

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Drug Information of FENOFIBRATE

Product NDC: 60760-900
Proprietary Name: FENOFIBRATE
Non Proprietary Name: FENOFIBRATE
Active Ingredient(s): 67    mg/1 & nbsp;   FENOFIBRATE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of FENOFIBRATE

Product NDC: 60760-900
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075868
Marketing Category: ANDA
Start Marketing Date: 20130502

Package Information of FENOFIBRATE

Package NDC: 60760-900-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-900-30)

NDC Information of FENOFIBRATE

NDC Code 60760-900-30
Proprietary Name FENOFIBRATE
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-900-30)
Product NDC 60760-900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENOFIBRATE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130502
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
Substance Name FENOFIBRATE
Strength Number 67
Strength Unit mg/1
Pharmaceutical Classes Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]

Complete Information of FENOFIBRATE


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