Last Updated: September 24, 2026

Details for New Drug Application (NDA): 220274

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NDA 220274 describes SODIUM ACETATE, which is a drug marketed by Amneal, Extrovis, Fresenius Kabi Usa, Hikma, Hospira, Milla Pharms, and Somerset Theraps Llc, and is included in seven NDAs. It is available from six suppliers. Additional details are available on the SODIUM ACETATE profile page.

The generic ingredient in SODIUM ACETATE is sodium acetate. There is one drug master file entry for this compound. Six suppliers are listed for this compound. Additional details are available on the sodium acetate profile page.

Summary for 220274

Tradename:	SODIUM ACETATE
Applicant:	Extrovis
Ingredient:	sodium acetate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	100MEQ/50ML (2MEQ/ML)
Approval Date:	Apr 17, 2026	TE:	AP	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	200MEQ/100ML (2MEQ/ML)
Approval Date:	Apr 17, 2026	TE:	AP	RLD:	No

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