DDAVP Detail

Drug Name(s):
DDAVP

FDA Application No.:
NDA 017922

Active Ingredient(s):
DESMOPRESSIN ACETATE

Company:
SANOFI AVENTIS US

Original Approval or Tentative Approval Date:
February 20, 1978

Products on Application NDA 017922:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DESMOPRESSIN ACETATE	0.01%	SOLUTION; NASAL	Prescription	none
DESMOPRESSIN ACETATE	0.01MG/SPRAY	SPRAY, METERED; NASAL	Prescription	AB

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last updated on 11-21-2008

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