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Last Updated: April 18, 2024

Details for New Drug Application (NDA): 021712

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NDA 021712 describes FLUXID, which is a drug marketed by Ucb Inc and is included in one NDA. Additional details are available on the FLUXID profile page.

The generic ingredient in FLUXID is famotidine. There are eighteen drug master file entries for this compound. One hundred and thirty-seven suppliers are listed for this compound. Additional details are available on the famotidine profile page.

Summary for 021712

Tradename:	FLUXID
Applicant:	Ucb Inc
Ingredient:	famotidine
Patents:	0
Formulation / Manufacturing:	see details

Medical Subject Heading (MeSH) Categories for 021712

Anti-Ulcer Agents
Histamine H2 Antagonists

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET, ORALLY DISINTEGRATING;ORAL			Strength	20MG
Approval Date:	Sep 24, 2004	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET, ORALLY DISINTEGRATING;ORAL			Strength	40MG
Approval Date:	Sep 24, 2004	TE:		RLD:	No

Expired US Patents for NDA 021712

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Ucb Inc	FLUXID	famotidine	TABLET, ORALLY DISINTEGRATING;ORAL	021712-002	Sep 24, 2004	⤷ Try a Trial	⤷ Try a Trial
Ucb Inc	FLUXID	famotidine	TABLET, ORALLY DISINTEGRATING;ORAL	021712-002	Sep 24, 2004	⤷ Try a Trial	⤷ Try a Trial
Ucb Inc	FLUXID	famotidine	TABLET, ORALLY DISINTEGRATING;ORAL	021712-001	Sep 24, 2004	⤷ Try a Trial	⤷ Try a Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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