VASOCIDIN Detail

Drug Name(s):
VASOCIDIN

FDA Application No.:
NDA 018988

Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

Company:
NOVARTIS

Original Approval or Tentative Approval Date:
August 25, 1988

Products on Application NDA 018988:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM	EQ 0.23% PHOSPHATE;10%	SOLUTION/DROPS; OPHTHALMIC	Prescription	AT

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last updated on 11-21-2008

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