Drug Details: OPTICROM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	OPTICROM
FDA Application No:	(NDA) 018155
Active Ingredient(s):	CROMOLYN SODIUM
Company:	ALLERGAN
Original Approval or Tentative Approval Date:	October 3, 1984
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug
	O Orphan drug

Therapeutic Equivalents	Labels are not available
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
OPTICROM	CROMOLYN SODIUM	4%	SOLUTION/DROPS; OPHTHALMIC	Prescription	Yes	AT

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