Last Updated: May 2, 2026

Details for New Drug Application (NDA): 019350

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NDA 019350 describes CUPRIC SULFATE, which is a drug marketed by Abraxis Pharm, Am Regent, and Apotex Corp, and is included in three NDAs. Additional details are available on the CUPRIC SULFATE profile page.

The generic ingredient in CUPRIC SULFATE is cupric sulfate. Additional details are available on the cupric sulfate profile page.

Summary for 019350

Tradename:	CUPRIC SULFATE
Applicant:	Abraxis Pharm
Ingredient:	cupric sulfate
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 0.4MG COPPER/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	May 5, 1987	TE:		RLD:	Yes

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