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Last Updated: December 26, 2024

Details for New Drug Application (NDA): 213864

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NDA 213864 describes FENOFIBRATE, which is a drug marketed by Sun Pharm Inds Ltd, Ajanta Pharma Ltd, Alembic, Amneal, Aurobindo Pharma, Austarpharma, Chartwell Rx, Cipla, Creekwood Pharms, Dr Reddys, Hetero Labs Ltd Iii, Impax Labs, Lupin Ltd, Mankind Pharma, Mylan, Mylan Pharms Inc, Prinston Inc, Rhodes Pharms, Rising, Sun Pharm, Valeant Pharms North, Yichang Humanwell, Ani Pharms, Apotex, Aurobindo Pharma Ltd, Chartwell, Dr Reddys Labs Sa, Glenmark Pharms Ltd, Invagen Pharms, Norvium Bioscience, Novast Labs, Reyoung, and Torrent, and is included in forty-six NDAs. It is available from forty-five suppliers. Additional details are available on the FENOFIBRATE profile page.

The generic ingredient in FENOFIBRATE is fenofibrate. There are forty-two drug master file entries for this compound. Fifty-three suppliers are listed for this compound. Additional details are available on the fenofibrate profile page.

Summary for 213864

Tradename:	FENOFIBRATE
Applicant:	Mankind Pharma
Ingredient:	fenofibrate
Patents:	0

Pharmacology for NDA: 213864

Medical Subject Heading (MeSH) Categories for 213864

Hypolipidemic Agents

Suppliers and Packaging for NDA: 213864

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
FENOFIBRATE	fenofibrate	TABLET;ORAL	213864	ANDA	Northwind Pharmaceuticals, LLC	51655-856	51655-856-52	30 TABLET in 1 BOTTLE, PLASTIC (51655-856-52)
FENOFIBRATE	fenofibrate	TABLET;ORAL	213864	ANDA	St. Mary's Medical Park Pharmacy	60760-318	60760-318-30	30 TABLET in 1 BOTTLE, PLASTIC (60760-318-30)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	54MG
Approval Date:	Jun 12, 2020	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	160MG
Approval Date:	Jun 12, 2020	TE:	AB	RLD:	No

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