DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METRONIDAZOLE
FDA Application No:
(ANDA) 070039
Active Ingredient(s):
METRONIDAZOLE
Company:
PAR PHARM
Label History
Labels are not available on this site for METRONIDAZOLE, (ANDA) 070039
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/16/1992
011
Labeling
11/1/1988
008
SBA
6/16/1988
006
Labeling
5/23/1986
003
Chemistry
5/23/1986
002
Chemistry
1/29/1985
000
Approval
Therapeutic Equivalents
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