Drug Details: ZERIT

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ZERIT
FDA Application No:	(NDA) 020413
Active Ingredient(s):	STAVUDINE
Company:	BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:	September 6, 1996
Chemical Type:	3 New dosage form
Review Classification:	P Priority review drug

Therapeutic Equivalents	Label Information
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
ZERIT	STAVUDINE	1MG/ML	FOR SOLUTION; ORAL	Prescription	Yes	None

Comments for ZERIT

Name: *

Email: *

Text:
(HTML OK)

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

There are no comments.