DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METOCLOPRAMIDE HYDROCHLORIDE
FDA Application No:
(ANDA) 072215
Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for METOCLOPRAMIDE HYDROCHLORIDE, (ANDA) 072215
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/13/1995
004
Labeling
10/21/1998
003
Chemistry
2/24/1992
002
Chemistry
9/18/1990
001
Labeling in Effect
1/30/1990
000
Approval
Therapeutic Equivalents
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