DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CHILDREN'S ADVIL
FDA Application No:
(NDA) 019833
Active Ingredient(s):
IBUPROFEN
Company:
WYETH CONS
Label History
Labels are not available on this site for CHILDREN'S ADVIL, (NDA) 019833
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/8/1998
012
Manufacturing Change or Addition
1/26/1998
011
Labeling Revision
Review
10/24/1994
008
Control Supplement
11/27/1991
007
Manufacturing Change or Addition
4/21/1994
005
Manufacturing Change or Addition
7/27/1994
002
Control Supplement
4/25/1994
001
Expiration Date Change
9/19/1989
000
Approval
There are no Therapeutic Equivalents
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