Drug History: BETAMETHASONE DIPROPIONATE

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	BETAMETHASONE DIPROPIONATE
FDA Application No:	(ANDA) 070281
Active Ingredient(s):	BETAMETHASONE DIPROPIONATE
Company:	ACTAVIS MID ATLANTIC

Label History

Labels are not available on this site for BETAMETHASONE DIPROPIONATE, (ANDA) 070281

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
7/19/1995	018	Labeling
12/23/1994	017	Chemistry
7/15/1992	016	Chemistry
4/6/1992	015	Chemistry in Effect
3/5/1991	014	Labeling
4/20/1992	013	Chemistry
9/28/1990	012	Chemistry
10/9/1990	010	Labeling
1/23/1991	009	Chemistry
2/15/1989	008	Chemistry
2/15/1989	007	Chemistry
2/15/1989	006	Chemistry
11/6/1987	004	Chemistry
10/9/1986	003	Chemistry
7/21/1986	001	Chemistry
7/31/1985	000	Approval

Therapeutic Equivalents

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