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Last Updated: December 18, 2025

Details for New Drug Application (NDA): 217624

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NDA 217624 describes ZINC SULFATE, which is a drug marketed by Abraxis Pharm, Am Regent, Apotex, Aspiro, Fresenius Kabi Usa, Gland, Nivagen Pharms Inc, Rk Pharma, Somerset Theraps Llc, and Zydus Pharms, and is included in ten NDAs. It is available from ten suppliers. Additional details are available on the ZINC SULFATE profile page.

The generic ingredient in ZINC SULFATE is zinc sulfate. There are thirty-eight drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the zinc sulfate profile page.

Summary for 217624

Tradename:	ZINC SULFATE
Applicant:	Rk Pharma
Ingredient:	zinc sulfate
Patents:	0

Medical Subject Heading (MeSH) Categories for 217624

Astringents

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	EQ 10MG BASE/10ML (EQ 1MG BASE/ML)
Approval Date:	Jun 10, 2025	TE:	AP	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	EQ 25MG BASE/5ML (EQ 5MG BASE/ML)
Approval Date:	Jun 10, 2025	TE:	AP	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	SOLUTION;INTRAVENOUS			Strength	EQ 30MG BASE/10ML (EQ 3MG BASE/ML)
Approval Date:	Jun 10, 2025	TE:	AP	RLD:	No

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