TECHNELITE Detail

Drug Name(s):
TECHNELITE

FDA Application No.:
NDA 017771

Active Ingredient(s):
TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR

Company:
BRISTOL MYERS SQUIBB

Original Approval or Tentative Approval Date:
November 15, 1976

Products on Application NDA 017771:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR	0.0083-2.7 CI/GENERATOR	SOLUTION; INJECTION, ORAL	Prescription	none

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last updated on 11-21-2008

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