Drug History: CARBIDOPA AND LEVODOPA

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	CARBIDOPA AND LEVODOPA
FDA Application No:	(ANDA) 075091
Active Ingredient(s):	CARBIDOPA; LEVODOPA
Company:	MYLAN

Label History

View the label approved on September 30, 1999 for CARBIDOPA AND LEVODOPA, (ANDA) 075091

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
10/1/2002	008	Control Supplement
6/12/2002	007	Expiration Date Change
11/7/2001	006	Labeling
8/11/2000	005	Control Supplement
8/11/2000	004	Control Supplement
2/4/2000	003	Labeling
4/21/2000	002	Labeling
4/21/2000	001	Chemistry New Strength
9/30/1999	000	Approval	Letter Label Review
2/26/1999	000	Tentative Approval	Letter Label Review

There are no Therapeutic Equivalents