DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
REGLAN
FDA Application No:
(NDA) 017862
Active Ingredient(s):
METOCLOPRAMIDE HYDROCHLORIDE
Company:
BAXTER HLTHCARE CORP
Original Approval or Tentative Approval Date:
February 7, 1979
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
REGLAN
METOCLOPRAMIDE HYDROCHLORIDE
EQ 5MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
REGLAN
METOCLOPRAMIDE HYDROCHLORIDE
EQ 10MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
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