Drug History: H.P. ACTHAR GEL

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	H.P. ACTHAR GEL
FDA Application No:	(NDA) 008372
Active Ingredient(s):	CORTICOTROPIN
Company:	QUESTCOR PHARMS

Label History

Labels are not available on this site for H.P. ACTHAR GEL, (NDA) 008372

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
11/6/2002	035	Expiration Date Change
7/15/1999	034	Manufacturing Change or Addition
12/15/1998	033	Package Change
4/5/1994	031	Package Change
3/26/1993	030	Package Change
4/22/1992	029	Labeling Revision
3/25/1985	028	Manufacturing Change or Addition
1/15/1985	027	Expiration Date Change
8/29/1984	026	Expiration Date Change
8/24/1983	025	Labeling Revision
3/26/1981	024	Labeling Revision
6/26/1979	022	Expiration Date Change
6/26/1979	021	Labeling Revision
6/26/1979	020	Distributor
6/26/1979	018	Labeling Revision
3/14/1978	017	Labeling Revision
10/5/1977	016	Labeling Revision
6/1/1977	015	Labeling Revision
4/29/1952	000	Approval

Therapeutic Equivalents

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