DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CLEMASTINE FUMARATE
FDA Application No:
(ANDA) 074075
Active Ingredient(s):
CLEMASTINE FUMARATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for CLEMASTINE FUMARATE, (ANDA) 074075
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/4/2000
008
Expiration Date Change
12/4/2000
007
Control Supplement
3/27/2000
006
Expiration Date Change
3/27/2000
005
Labeling
3/27/2000
004
Packaging Addition
2/8/1994
001
Labeling
10/31/1993
000
Approval
Therapeutic Equivalents
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