NAPROXEN SODIUM Detail

Drug Name(s):
NAPROXEN SODIUM

FDA Application No.:
NDA 074198

Active Ingredient(s):
NAPROXEN SODIUM

Company:
TEVA

Original Approval or Tentative Approval Date:
December 20, 1993

Products on Application NDA 074198:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NAPROXEN SODIUM	EQ 500MG BASE	TABLET; ORAL	Prescription	AB

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.

Navigation

Resources

Medical Dictionary

Drug Information

Events

«	December 2008
S	M	T	W	T	F	S
	1	2	3	4	5	6
7	8	9	10	11	12	13
14	15	16	17	18	19	20
21	22	23	24	25	26	27
28	29	30	31

Job search

Find jobs in healthcare or get job search tips

About | Privacy Statement | Terms & Conditions | Contact Us | Link Resources

Medicine.org is an online community where consumers can share health resources and information. It is intended to supplement, not replace, professional medical care. Always consult your doctor for medical advice related to your specific health condition.

We comply with the HONcode standard for health trust worthy information:
verify here.

Links to Site

last updated on 12-01-2008

NAPROXEN SODIUM Detail

Hot Topics

Sponsored Links

Recall Notices

Action Alerts

Most Recent Content

Active forum topics

Poll

Subscribe to our feed