DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SEMPREX-D
FDA Application No:
(NDA) 019806
Active Ingredient(s):
ACRIVASTINE; PSEUDOEPHEDRINE HYDROCHLORIDE
Company:
UCB INC
Label History
Labels are not available on this site for SEMPREXD, (NDA) 019806
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/25/2004
008
Labeling Revision
Letter
2/20/2002
005
Control Supplement
1/21/2000
004
Expiration Date Change
12/4/1997
003
Control Supplement
7/30/1996
002
Manufacturing Change or Addition
9/23/1994
001
Labeling Revision
3/25/1994
000
Approval
There are no Therapeutic Equivalents
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