Details for New Drug Application (NDA): 020121

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NDA 020121 describes FLONASE, which is a drug marketed by Haleon Us Holdings and is included in three NDAs. There are four patents protecting this drug. Additional details are available on the FLONASE profile page.

The generic ingredient in FLONASE is fluticasone furoate. There are twenty-nine drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the fluticasone furoate profile page.

Summary for 020121

Tradename:	FLONASE
Applicant:	Haleon Us Holdings
Ingredient:	fluticasone propionate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SPRAY, METERED;NASAL			Strength	0.05MG/SPRAY Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Oct 19, 1994	TE:		RLD:	Yes

Expired US Patents for NDA 020121

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Haleon Us Holdings	FLONASE	fluticasone propionate	SPRAY, METERED;NASAL	020121-001	Oct 19, 1994	⤷ Subscribe	⤷ Subscribe
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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