Drug Details: NAPHCON FORTE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	NAPHCON FORTE
FDA Application No:	(ANDA) 080229
Active Ingredient(s):	NAPHAZOLINE HYDROCHLORIDE
Company:	ALCON
Original Approval or Tentative Approval Date:	March 6, 1974

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
NAPHCON FORTE	NAPHAZOLINE HYDROCHLORIDE	0.1%	SOLUTION/DROPS; OPHTHALMIC	Discontinued	No	None

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