DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEDIPREN
FDA Application No:
(ANDA) 071215
Active Ingredient(s):
IBUPROFEN
Company:
MCNEIL
Label History
Labels are not available on this site for MEDIPREN, (ANDA) 071215
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/29/1988
020
Chemistry
12/29/1988
020
Labeling
2/14/1989
019
Chemistry
9/9/1988
017
Labeling
4/7/1988
016
Chemistry
4/7/1988
015
Chemistry
4/7/1988
014
Chemistry
10/20/1987
011
Chemistry
9/10/1987
006
Chemistry
9/10/1987
005
Chemistry
11/5/1986
004
Chemistry
11/5/1986
003
Chemistry
11/5/1986
002
Chemistry
6/26/1986
000
Approval
Therapeutic Equivalents
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