Drug Details: LASIX

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	LASIX
FDA Application No:	(NDA) 016363
Active Ingredient(s):	FUROSEMIDE
Company:	SANOFI AVENTIS US
Original Approval or Tentative Approval Date:	March 20, 1968
Chemical Type:	3 New dosage form
Review Classification:	P Priority review drug

There are no Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
LASIX	FUROSEMIDE	10MG/ML Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	INJECTABLE; INJECTION	Discontinued	No	None

Comments for LASIX

Name: *

Email: *

Text:
(HTML OK)

Enter the code from the picture: *
(click here to load another image)

There are no comments.