DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KEMADRIN
FDA Application No:
(NDA) 009818
Active Ingredient(s):
PROCYCLIDINE HYDROCHLORIDE
Company:
MONARCH PHARMS
Label History
Labels are not available on this site for KEMADRIN, (NDA) 009818
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/3/1982
015
Package Change
2/19/1980
013
Manufacturing Change or Addition
6/14/1979
011
Manufacturing Change or Addition
4/10/1978
010
Expiration Date Change
4/10/1978
009
Package Change
2/9/1977
008
Package Change
9/27/1976
007
Control Supplement
11/25/1974
006
Control Supplement
7/27/1955
000
Approval
There are no Therapeutic Equivalents
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