Drug Details: RESTASIS

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	RESTASIS
FDA Application No:	(NDA) 050790
Active Ingredient(s):	CYCLOSPORINE
Company:	ALLERGAN
Original Approval or Tentative Approval Date:	December 23, 2002
Chemical Type:	3 New dosage form
Review Classification:	P Priority review drug

Therapeutic Equivalents	Label Information
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
RESTASIS	CYCLOSPORINE	0.05%	EMULSION; OPHTHALMIC	Prescription	Yes	None

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