Drug Details: FLURBIPROFEN SODIUM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	FLURBIPROFEN SODIUM
FDA Application No:	(ANDA) 074447
Active Ingredient(s):	FLURBIPROFEN SODIUM
Company:	BAUSCH AND LOMB
Original Approval or Tentative Approval Date:	January 4, 1995

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
FLURBIPROFEN SODIUM	FLURBIPROFEN SODIUM	0.03%	SOLUTION/DROPS; OPHTHALMIC	Prescription	No	AT

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