Drug History: NALOXONE

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	NALOXONE
FDA Application No:	(ANDA) 070190
Active Ingredient(s):	NALOXONE HYDROCHLORIDE
Company:	WYETH AYERST

Label History

Labels are not available on this site for NALOXONE, (ANDA) 070190

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
6/3/1988	003	Labeling
2/20/1987	002	Chemistry
10/2/1985	000	Approval

Therapeutic Equivalents

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