Drug History: PROVENTIL-HFA

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:	PROVENTIL-HFA
FDA Application No:	(NDA) 020503
Active Ingredient(s):	ALBUTEROL SULFATE
Company:	3M

Label History

View the label approved on September 23, 1998 for PROVENTILHFA, (NDA) 020503

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
1/29/2004	022	Labeling Revision	Letter
7/26/2002	021	Manufacturing Change or Addition
1/17/2002	020	Control Supplement
4/17/2001	019	Manufacturing Change or Addition
1/10/2002	018	Control Supplement
10/5/2000	017	Control Supplement
9/28/2000	016	Control Supplement
1/18/2002	015	Control Supplement
6/16/2000	014	Control Supplement
3/13/2000	013	Control Supplement
4/12/2000	012	Control Supplement
6/2/1999	011	New or Modified Indication	Letter Review
8/18/1999	010	Control Supplement
4/4/2000	009	Control Supplement
6/17/1999	008	Control Supplement
3/12/1998	007	Control Supplement
6/16/2000	006	Control Supplement
2/5/1998	005	Control Supplement
9/23/1998	004	New or Modified Indication	Letter Label Review
8/18/1997	003	Manufacturing Change or Addition
4/22/1997	002	Labeling Revision
12/26/1996	001	Control Supplement
8/15/1996	000	Approval

Therapeutic Equivalents