DEXTROSE 5% AND SODIUM CHLORIDE 0.9% Drug Patent Profile

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Dextrose 5% And Sodium Chloride 0.9% is a drug marketed by Fresenius Kabi Usa, Abbott, B Braun, Icu Medical Inc, and Miles. and is included in six NDAs.

The generic ingredient in DEXTROSE 5% AND SODIUM CHLORIDE 0.9% is dextrose; sodium chloride. There are nine drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the dextrose; sodium chloride profile page.

US Patents:	0
Applicants:	5
NDAs:	6
Finished Product Suppliers / Packagers:	3
DailyMed Link:	DEXTROSE 5% AND SODIUM CHLORIDE 0.9% at DailyMed

Drug Class	Osmotic Laxative
Mechanism of Action	Osmotic Activity
Physiological Effect	Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Fresenius Kabi Usa	DEXTROSE 5% AND SODIUM CHLORIDE 0.9%	dextrose; sodium chloride	INJECTABLE;INJECTION	211211-001	Sep 14, 2020	AP	RX	No	No	⤷ Sign Up	⤷ Sign Up				⤷ Sign Up
B Braun	DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	dextrose; sodium chloride	INJECTABLE;INJECTION	019631-010	Feb 24, 1988	AP	RX	No	No	⤷ Sign Up	⤷ Sign Up				⤷ Sign Up
Abbott	DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	dextrose; sodium chloride	INJECTABLE;INJECTION	019483-001	Oct 4, 1985		DISCN	No	No	⤷ Sign Up	⤷ Sign Up				⤷ Sign Up
B Braun	DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	dextrose; sodium chloride	INJECTABLE;INJECTION	018026-001	Approved Prior to Jan 1, 1982		DISCN	No	No	⤷ Sign Up	⤷ Sign Up				⤷ Sign Up
Miles	DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	dextrose; sodium chloride	INJECTABLE;INJECTION	018500-001	Approved Prior to Jan 1, 1982		DISCN	No	No	⤷ Sign Up	⤷ Sign Up				⤷ Sign Up
Icu Medical Inc	DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	dextrose; sodium chloride	INJECTABLE;INJECTION	017585-001	Approved Prior to Jan 1, 1982	AP	RX	Yes	Yes	⤷ Sign Up	⤷ Sign Up				⤷ Sign Up
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>TE	>Type	>RLD	>RS	>Patent No.	>Patent Expiration	>Product	>Substance	>Delist Req.	>Exclusivity Expiration