DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RANITIDINE
FDA Application No:
(ANDA) 074764
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
BEDFORD
Original Approval or Tentative Approval Date:
November 19, 2004
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
RANITIDINE
RANITIDINE HYDROCHLORIDE
EQ 25MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
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