MAGNESIUM SULFATE Detail

Drug Name(s):
MAGNESIUM SULFATE

FDA Application No.:
NDA 019316

Active Ingredient(s):
MAGNESIUM SULFATE

Company:
ABRAXIS PHARM

Original Approval or Tentative Approval Date:
September 7, 1986

Products on Application NDA 019316:

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

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last updated on 11-21-2008

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