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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 018988

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NDA 018988 describes VASOCIDIN, which is a drug marketed by Novartis and is included in two NDAs. Additional details are available on the VASOCIDIN profile page.

The generic ingredient in VASOCIDIN 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 018988

Tradename:	VASOCIDIN
Applicant:	Novartis
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		Strength	EQ 0.23% PHOSPHATE;10% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Aug 26, 1988	TE:		RLD:	Yes

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