Drug History: MAOLATE

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:	MAOLATE
FDA Application No:	(NDA) 014217
Active Ingredient(s):	CHLORPHENESIN CARBAMATE
Company:	PHARMACIA AND UPJOHN

Label History

Labels are not available on this site for MAOLATE, (NDA) 014217

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
5/15/1981	021	Labeling Revision
11/24/1975	018	Labeling Revision
6/14/1965	000	Approval

There are no Therapeutic Equivalents

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