Drug History: OCL

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:	OCL
FDA Application No:	(NDA) 019284
Active Ingredient(s):	POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE
Company:	HOSPIRA

Label History

Labels are not available on this site for OCL, (NDA) 019284

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
8/17/2000	014	Control Supplement
11/4/1999	012	Control Supplement
2/3/1998	010	Package Change
7/30/1996	008	Control Supplement
4/13/1992	006	Package Change
11/22/1988	005	Labeling Revision
9/30/1988	004	Expiration Date Change
11/25/1987	003	Labeling Revision
9/30/1988	001	Manufacturing Change or Addition
4/30/1986	000	Approval

There are no Therapeutic Equivalents

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