Drug Details: DIAMOX

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	DIAMOX
FDA Application No:	(NDA) 008943
Active Ingredient(s):	ACETAZOLAMIDE
Company:	DURAMED PHARMS BARR
Original Approval or Tentative Approval Date:	July 27, 1953
Chemical Type:	1 New molecular entity (NME)
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
DIAMOX	ACETAZOLAMIDE	125MG	TABLET; ORAL	Discontinued	No	None
DIAMOX	ACETAZOLAMIDE	250MG	TABLET; ORAL	Discontinued	No	None

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