GENTAMICIN SULFATE Detail

Drug Name(s):
GENTAMICIN SULFATE

FDA Application No.:
NDA 062251

Active Ingredient(s):
GENTAMICIN SULFATE

Company:
BAXTER HLTHCARE

Original Approval or Tentative Approval Date:
May 21, 1987

Products on Application NDA 062251:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GENTAMICIN SULFATE	EQ 10MG BASE/ML	INJECTABLE; INJECTION	Discontinued	none

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January 2009

GENTAMICIN SULFATE Detail

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