MAGNESIUM SULFATE Detail

Drug Name(s):
MAGNESIUM SULFATE

FDA Application No.:
NDA 075151

Active Ingredient(s):
MAGNESIUM SULFATE

Company:
HOSPIRA

Original Approval or Tentative Approval Date:
April 24, 2000

Products on Application NDA 075151:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
MAGNESIUM SULFATE	500MG/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008