GENTAMICIN SULFATE Detail

Drug Name(s):
GENTAMICIN SULFATE

FDA Application No.:
NDA 065121

Active Ingredient(s):
GENTAMICIN SULFATE

Company:
ALTANA

Original Approval or Tentative Approval Date:
January 29, 2004

Products on Application NDA 065121:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GENTAMICIN SULFATE	EQ 0.3% BASE	SOLUTION/DROPS; OPHTHALMIC	Prescription	AT

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January 2009

GENTAMICIN SULFATE Detail

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