GENTAMICIN SULFATE Detail

Drug Name(s):
GENTAMICIN SULFATE

FDA Application No.:
NDA 062366

Active Ingredient(s):
GENTAMICIN SULFATE

Company:
ABRAXIS PHARM

Original Approval or Tentative Approval Date:
November 25, 1991

Products on Application NDA 062366:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GENTAMICIN SULFATE	EQ 40MG BASE/ML	INJECTABLE; INJECTION	Prescription	AP

Welcome

Did you know it can take decades for medical innovations to be widely adopted by the healthcare community? To make the best decisions for your health, you need more information than your physician alone can provide. Medicine.org is here to help you become an advocate for your own health by allowing you to share and discover the current healthcare information you need. Learn more.

January 2009

GENTAMICIN SULFATE Detail

Sponsored Links

Recall Notices

Action Alerts

Active forum topics

Poll

Subscribe to our feed

Welcome

Diseases & Conditions

Navigation

Resources

Medical Dictionary

Drug Information

Events

Who's online

Job search