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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 073630

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NDA 073630 describes SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE, which is a drug marketed by Bausch And Lomb and Genus and is included in two NDAs. It is available from two suppliers. Additional details are available on the SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE profile page.

The generic ingredient in SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE 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 073630

Tradename:	SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
Applicant:	Genus
Ingredient:	prednisolone sodium phosphate; sulfacetamide sodium
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION/DROPS;OPHTHALMIC			Strength	EQ 0.23% PHOSPHATE;10%
Approval Date:	May 27, 1993	TE:		RLD:	No

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