Drug Details: NEGGRAM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	NEGGRAM
FDA Application No:	(NDA) 017430
Active Ingredient(s):	NALIDIXIC ACID
Company:	SANOFI AVENTIS US
Original Approval or Tentative Approval Date:	April 17, 1973
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no 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
NEGGRAM	NALIDIXIC ACID	250MG/5ML	SUSPENSION; ORAL	Discontinued	No	None

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