DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CYCLOPENTOLATE HYDROCHLORIDE
FDA Application No:
(ANDA) 089162
Active Ingredient(s):
CYCLOPENTOLATE HYDROCHLORIDE
Company:
ALCON UNIVERSAL
Label History
Labels are not available on this site for CYCLOPENTOLATE HYDROCHLORIDE, (ANDA) 089162
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/7/1996
004
Chemistry
6/7/1996
003
Chemistry
4/16/1996
002
Chemistry
6/20/1994
001
Labeling
1/24/1991
000
Approval
Therapeutic Equivalents
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