NDC 65862-769

Fenofibrate

Fenofibrate

Fenofibrate is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Fenofibrate.

Product ID65862-769_0d0c4d72-5837-4642-9c8d-ad6819ef2b1f
NDC65862-769
Product TypeHuman Prescription Drug
Proprietary NameFenofibrate
Generic NameFenofibrate
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2016-05-05
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA205118
Labeler NameAurobindo Pharma Limited
Substance NameFENOFIBRATE
Active Ingredient Strength145 mg/1
Pharm ClassesPeroxisome Prol
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 65862-769-01

100 TABLET, COATED in 1 BOTTLE (65862-769-01)
Marketing Start Date2016-05-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-769-01 [65862076901]

Fenofibrate TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-05

NDC 65862-769-05 [65862076905]

Fenofibrate TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-05

NDC 65862-769-78 [65862076978]

Fenofibrate TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-05

NDC 65862-769-99 [65862076999]

Fenofibrate TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-05

NDC 65862-769-10 [65862076910]

Fenofibrate TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205118
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-05

NDC 65862-769-90 [65862076990]

Fenofibrate TABLET, COATED
Marketing CategoryANDA
Application NumberANDA205118
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-05-05

Drug Details

Active Ingredients

IngredientStrength
FENOFIBRATE145 mg/1

Medicade Reported Pricing

65862076990 FENOFIBRATE 145 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Fenofibrate" or generic name "Fenofibrate"

NDCBrand NameGeneric Name
0093-7755FenofibrateFenofibrate
0093-7756FenofibrateFenofibrate
0115-0511FenofibrateFENOFIBRATE
0115-0522FenofibrateFENOFIBRATE
0115-0533FenofibrateFENOFIBRATE
0115-1522FenofibrateFenofibrate
0115-1523FenofibrateFenofibrate
0115-5511FENOFIBRATEFENOFIBRATE
0115-5522FENOFIBRATEFENOFIBRATE
68071-2021FenofibrateFenofibrate
68071-1601FenofibrateFenofibrate
68071-2135FenofibrateFenofibrate
68071-3300FenofibrateFenofibrate
68071-3114fenofibratefenofibrate
68071-2042FenofibrateFenofibrate
68071-2115FenofibrateFenofibrate
68071-4264FenofibrateFenofibrate
68071-4289FenofibrateFenofibrate
68071-4297FenofibrateFenofibrate
68071-4320fenofibratefenofibrate
68071-4310FenofibrateFenofibrate
68071-4486FenofibrateFenofibrate
68071-4088FenofibrateFenofibrate
68071-4182fenofibratefenofibrate
68071-4265fenofibratefenofibrate
68071-4692FenofibrateFenofibrate
68071-4557FENOFIBRATEFENOFIBRATE
68071-4358fenofibratefenofibrate
68071-4659FenofibrateFenofibrate
68084-636FenofibrateFenofibrate
68084-328FENOFIBRATEFENOFIBRATE
68084-827FENOFIBRATEFENOFIBRATE
68084-329FenofibrateFenofibrate
68084-635FenofibrateFenofibrate
68084-835FenofibrateFenofibrate
68151-4717FenofibrateFenofibrate
68151-4718FenofibrateFenofibrate
68180-130FenofibrateFenofibrate
68180-131FenofibrateFenofibrate
68180-360FenofibrateFenofibrate
68180-363FenofibrateFenofibrate
68180-362FenofibrateFenofibrate
68180-361FenofibrateFenofibrate
68382-270FenofibrateFenofibrate
68382-269FenofibrateFenofibrate
68462-581fenofibratefenofibrate
68462-582fenofibratefenofibrate
68462-580fenofibratefenofibrate
68788-7000FenofibrateFenofibrate
68788-6330FenofibrateFenofibrate

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