Drug History: BETIMOL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	BETIMOL
FDA Application No:	(NDA) 020439
Active Ingredient(s):	TIMOLOL
Company:	SANTEN OY

Label History

View the label approved on November 1, 2004 for BETIMOL, (NDA) 020439

To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
10/21/2004	011	Labeling Revision	Letter Label
2/8/2002	009	Control Supplement
7/19/2001	008	Control Supplement
11/30/1999	006	Manufacturing Change or Addition
4/5/1999	005	Labeling Revision
3/8/1999	004	Expiration Date Change
9/4/1998	003	Control Supplement
11/3/1997	002	Labeling Revision
1/31/1997	001	Expiration Date Change
3/31/1995	000	Approval

There are no Therapeutic Equivalents