Drug History: ISUPREL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	ISUPREL
FDA Application No:	(NDA) 010515
Active Ingredient(s):	ISOPROTERENOL HYDROCHLORIDE
Company:	HOSPIRA

Label History

View the label approved on May 4, 1999 for ISUPREL, (NDA) 010515

To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
7/18/2001	024	Manufacturing Change or Addition
2/23/2000	023	Labeling Revision
5/4/1999	022	New or Modified Indication	Letter Label Review
2/14/1996	021	Labeling Revision
3/9/1992	020	Control Supplement
2/14/1996	019	Labeling Revision
2/6/1989	018	Labeling Revision
7/24/1987	017	Labeling Revision
12/8/1987	016	Labeling Revision
9/26/1984	015	Control Supplement
10/8/1986	014	Practioner Draft Labeling
8/11/1978	013	Expiration Date Change
8/4/1978	012	Control Supplement
9/5/1979	011	Labeling Revision
10/8/1986	007	New or Modified Indication
2/6/1974	006	Labeling Revision
5/25/1956	000	Approval

Therapeutic Equivalents