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Last Updated: March 19, 2026

Details for New Drug Application (NDA): 078668

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NDA 078668 describes SULFACETAMIDE SODIUM, which is a drug marketed by Fougera Pharms, Padagis Us, Sun Pharma Canada, Alcon Pharms Ltd, Bausch And Lomb, Chartwell Rx, Epic Pharma Llc, Pharmafair, Pharmobedient, and Genus, and is included in twelve NDAs. It is available from seven suppliers. Additional details are available on the SULFACETAMIDE SODIUM profile page.

The generic ingredient in SULFACETAMIDE SODIUM is prednisolone sodium phosphate; sulfacetamide sodium. There are eighty-eight drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the prednisolone sodium phosphate; sulfacetamide sodium profile page.

Summary for 078668

Tradename:	SULFACETAMIDE SODIUM
Applicant:	Sun Pharma Canada
Ingredient:	sulfacetamide sodium
Patents:	0

Medical Subject Heading (MeSH) Categories for 078668

Anti-Infective Agents, Local
Anti-Infective Agents, Urinary

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	LOTION;TOPICAL			Strength	10%
Approval Date:	May 20, 2009	TE:		RLD:	No

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