DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
METOCLOPRAMIDE
FDA Application No:
(ANDA) 077878
Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE
Company:
VINTAGE PHARMS
Original Approval or Tentative Approval Date:
August 28, 2006
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
METOCLOPRAMIDE
METOCLOPRAMIDE HYDROCHLORIDE
EQ 5MG BASE
TABLET; ORAL
Prescription
No
AB
METOCLOPRAMIDE
METOCLOPRAMIDE HYDROCHLORIDE
EQ 10MG BASE
TABLET; ORAL
Prescription
No
AB
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