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Last Updated: December 15, 2025

Details for New Drug Application (NDA): 210670

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NDA 210670 describes FENOFIBRATE, which is a drug marketed by Sun Pharm Inds Ltd, Ajanta Pharma Ltd, Alembic, Amneal, Aurobindo Pharma, Bausch, Bostal, Chartwell Rx, Cipla, Creekwood Pharms, Dr Reddys, Hetero Labs Ltd Iii, Impax Labs, Lupin Ltd, Macleods Pharms Ltd, Mankind Pharma, Mylan, Mylan Pharms Inc, Prinston Inc, Rhodes Pharms, Rising, Sun Pharm, Yichang Humanwell, Ani Pharms, Apotex, Aurobindo Pharma Ltd, Chartwell, Glenmark Pharms Ltd, Invagen Pharms, Novast Labs, Pharmobedient, Reyoung, and Torrent, and is included in forty-seven NDAs. It is available from forty-seven 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-six suppliers are listed for this compound. Additional details are available on the fenofibrate profile page.

Summary for 210670

Tradename:	FENOFIBRATE
Applicant:	Dr Reddys
Ingredient:	fenofibrate
Patents:	0

Pharmacology for NDA: 210670

Medical Subject Heading (MeSH) Categories for 210670

Hypolipidemic Agents

Suppliers and Packaging for NDA: 210670

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
FENOFIBRATE	fenofibrate	TABLET;ORAL	210670	ANDA	Dr. Reddy's Laboratories Inc.	43598-909	43598-909-90	90 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)
FENOFIBRATE	fenofibrate	TABLET;ORAL	210670	ANDA	Dr. Reddy's Laboratories Inc.	43598-910	43598-910-05	500 TABLET, FILM COATED in 1 BOTTLE (43598-910-05)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	54MG
Approval Date:	Sep 6, 2019	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	160MG
Approval Date:	Sep 6, 2019	TE:	AB	RLD:	No

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