Details for New Drug Application (NDA): 020559

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NDA 020559 describes TRITEC, which is a drug marketed by Glaxosmithkline and is included in one NDA. Additional details are available on the TRITEC profile page.

The generic ingredient in TRITEC is ranitidine bismuth citrate. There are forty-three drug master file entries for this compound. Additional details are available on the ranitidine bismuth citrate profile page.

Summary for 020559

Tradename:	TRITEC
Applicant:	Glaxosmithkline
Ingredient:	ranitidine bismuth citrate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	400MG
Approval Date:	Aug 8, 1996	TE:		RLD:	No

Expired US Patents for NDA 020559

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Glaxosmithkline	TRITEC	ranitidine bismuth citrate	TABLET;ORAL	020559-001	Aug 8, 1996	5,629,297	⤷ Subscribe
Glaxosmithkline	TRITEC	ranitidine bismuth citrate	TABLET;ORAL	020559-001	Aug 8, 1996	5,008,256	⤷ Subscribe
Glaxosmithkline	TRITEC	ranitidine bismuth citrate	TABLET;ORAL	020559-001	Aug 8, 1996	5,601,848	⤷ Subscribe
Glaxosmithkline	TRITEC	ranitidine bismuth citrate	TABLET;ORAL	020559-001	Aug 8, 1996	5,456,925	⤷ Subscribe
Glaxosmithkline	TRITEC	ranitidine bismuth citrate	TABLET;ORAL	020559-001	Aug 8, 1996	5,407,688	⤷ Subscribe
Glaxosmithkline	TRITEC	ranitidine bismuth citrate	TABLET;ORAL	020559-001	Aug 8, 1996	5,256,684	⤷ Subscribe
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