DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HETRAZAN
FDA Application No:
(NDA) 006459
Active Ingredient(s):
DIETHYLCARBAMAZINE CITRATE
Company:
LEDERLE
Label History
Labels are not available on this site for HETRAZAN, (NDA) 006459
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/10/1991
007
Manufacturing Change or Addition
2/28/1991
006
Expiration Date Change
6/7/1985
005
Manufacturing Change or Addition
6/7/1985
004
Control Supplement
6/7/1985
003
Control Supplement
6/7/1985
002
Labeling Revision
11/13/1950
000
Approval
There are no Therapeutic Equivalents
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