Drug History: PARAPLATIN

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	PARAPLATIN
FDA Application No:	(NDA) 019880
Active Ingredient(s):	CARBOPLATIN
Company:	BRISTOL MYERS SQUIBB

Label History

View the label approved on April 7, 2003 for PARAPLATIN, (NDA) 019880

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
3/21/2002	018	Package Change
11/2/2000	017	Manufacturing Change or Addition
4/30/2001	016	Labeling Revision
9/14/2000	015	Package Change
9/7/2000	014	Manufacturing Change or Addition
12/3/1999	013	Labeling Revision
4/30/2001	012	Labeling Revision
2/14/2002	011	Labeling Revision	Letter
11/15/1999	010	Labeling Revision
1/6/1998	009	Labeling Revision	Review
3/17/1995	008	Labeling Revision
2/23/1993	007	Labeling Revision
8/17/1990	004	Manufacturing Change or Addition
6/12/1990	003	Control Supplement
7/5/1991	001	New or Modified Indication	Label
3/3/1989	000	Approval

Therapeutic Equivalents