DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
COLESTID
FDA Application No:
(NDA) 020222
Active Ingredient(s):
COLESTIPOL HYDROCHLORIDE
Company:
PHARMACIA AND UPJOHN
Label History
Labels are not available on this site for COLESTID, (NDA) 020222
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/12/2002
002
Manufacturing Change or Addition
9/22/1995
001
Labeling Revision
7/19/1994
000
Approval
Therapeutic Equivalents
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