Drug History: INFLAMASE FORTE

Drugs Directory of False Positives

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	INFLAMASE FORTE
FDA Application No:	(ANDA) 080751
Active Ingredient(s):	PREDNISOLONE SODIUM PHOSPHATE
Company:	NOVARTIS

Label History

Labels are not available on this site for INFLAMASE FORTE, (ANDA) 080751

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
4/19/2001	022	Facility Addition
10/15/1996	021	Labeling
10/15/1996	020	Chemistry
6/10/1994	019	Microbiology
10/26/1994	018	Chemistry
11/2/1992	017	Labeling
4/1/1991	016	Labeling
6/2/1989	015	Chemistry
6/2/1989	014	Chemistry
6/2/1989	013	Chemistry
6/2/1989	012	Chemistry
6/2/1989	011	Chemistry
6/2/1989	010	Labeling
6/17/1988	009	Labeling
8/15/1986	008	Chemistry
12/19/1973	000	Approval

Therapeutic Equivalents

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