DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MEPERIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 073444
Active Ingredient(s):
MEPERIDINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for MEPERIDINE HYDROCHLORIDE, (ANDA) 073444
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/19/1999
008
Microbiology
2/2/1999
005
Microbiology
12/4/1996
004
Microbiology
8/18/1995
003
Chemistry
8/18/1995
002
Labeling
7/12/1995
001
Chemistry
3/17/1992
000
Approval
Therapeutic Equivalents
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