Drug History: NICARDIPINE HYDROCHLORIDE

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	NICARDIPINE HYDROCHLORIDE
FDA Application No:	(ANDA) 074670
Active Ingredient(s):	NICARDIPINE HYDROCHLORIDE
Company:	WATSON LABS

Label History

Labels are not available on this site for NICARDIPINE HYDROCHLORIDE, (ANDA) 074670

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
7/17/1998	004	Chemistry
8/14/1998	003	Chemistry
8/14/1998	002	Chemistry
10/28/1996	000	Approval

Therapeutic Equivalents

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