Drug Details: ULTIVA

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ULTIVA
FDA Application No:	(NDA) 020630
Active Ingredient(s):	REMIFENTANIL HYDROCHLORIDE
Company:	ABBOTT
Original Approval or Tentative Approval Date:	July 12, 1996
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
ULTIVA	REMIFENTANIL HYDROCHLORIDE	EQ 1MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	No	None
ULTIVA	REMIFENTANIL HYDROCHLORIDE	EQ 2MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	No	None
ULTIVA	REMIFENTANIL HYDROCHLORIDE	EQ 5MG BASE/VIAL	INJECTABLE; INJECTION	Prescription	Yes	None

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