Drug History: MIOSTAT

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Label and Approval History

Drug Name:	MIOSTAT
FDA Application No:	(NDA) 016968
Active Ingredient(s):	CARBACHOL
Company:	ALCON

Label History

View the label approved on November 16, 2004 for MIOSTAT, (NDA) 016968

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
11/10/2004	022	Labeling Revision	Letter Label
11/25/2002	020	Labeling Revision	Letter Label
12/18/2001	019	Control Supplement
10/18/1999	018	Package Change
4/15/1999	017	Package Change
5/2/1997	016	Control Supplement
1/14/1997	015	Control Supplement
6/26/1996	014	Control Supplement
8/18/1995	013	New or Modified Indication
12/14/1989	012	Labeling Revision
8/13/1984	009	Labeling Revision
12/6/1983	008	Expiration Date Change
5/16/1983	007	Formulation Revision
4/24/1980	006	Labeling Revision
4/24/1980	005	Expiration Date Change
6/12/1978	004	Formulation Revision
6/12/1978	003	Package Change
8/8/1978	002	Package Change
9/28/1972	000	Approval

Therapeutic Equivalents