GENTAMICIN SULFATE Detail

Drug Name(s):
GENTAMICIN SULFATE

FDA Application No.:
NDA 062318

Active Ingredient(s):
GENTAMICIN SULFATE

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
August 19, 1981

Products on Application NDA 062318:

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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