Drug Details: LANTUS

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	LANTUS
FDA Application No:	(NDA) 021081
Active Ingredient(s):	INSULIN GLARGINE RECOMBINANT
Company:	SANOFI AVENTIS US
Original Approval or Tentative Approval Date:	April 20, 2000
Chemical Type:	1 New molecular entity (NME)
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
LANTUS	INSULIN GLARGINE RECOMBINANT	100 UNITS/ML	INJECTABLE; INJECTION	Prescription	Yes	None

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