Drug Details: PROPOXYPHENE HYDROCHLORIDE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	PROPOXYPHENE HYDROCHLORIDE
FDA Application No:	(ANDA) 083186
Active Ingredient(s):	PROPOXYPHENE HYDROCHLORIDE
Company:	MUTUAL PHARM
Original Approval or Tentative Approval Date:	December 18, 1972

Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
PROPOXYPHENE HYDROCHLORIDE	PROPOXYPHENE HYDROCHLORIDE	65MG	CAPSULE; ORAL	Discontinued	No	None

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