Drug History: PROPOXYPHENE HYDROCHLORIDE

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	PROPOXYPHENE HYDROCHLORIDE
FDA Application No:	(ANDA) 083125
Active Ingredient(s):	PROPOXYPHENE HYDROCHLORIDE
Company:	SANDOZ

Label History

Labels are not available on this site for PROPOXYPHENE HYDROCHLORIDE, (ANDA) 083125

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
10/14/1998	079	Chemistry
8/31/1990	078	Labeling
1/6/1989	077	Labeling
1/15/1988	076	Chemistry
1/15/1988	075	Chemistry
6/9/1987	073	Chemistry
4/29/1987	072	Chemistry
1/15/1987	071	Chemistry
2/15/1984	069	Chemistry
2/15/1984	067	Chemistry
8/11/1983	066	Chemistry
8/11/1983	065	Chemistry
8/11/1983	064	Chemistry
8/9/1982	060	Chemistry
6/10/1982	059	Chemistry
6/10/1982	057	Chemistry
8/9/1982	055	Chemistry
6/10/1982	052	Chemistry
10/18/1972	000	Approval

Therapeutic Equivalents

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