OMNIPEN-N Detail

Drug Name(s):
OMNIPEN-N

FDA Application No.:
NDA 062718

Active Ingredient(s):
AMPICILLIN SODIUM

Company:
WYETH AYERST

Products on Application NDA 062718:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AMPICILLIN SODIUM	EQ 1GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none
AMPICILLIN SODIUM	EQ 250MG BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none

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

OMNIPEN-N 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