DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RANITIDINE HYDROCHLORIDE
FDA Application No:
(ANDA) 078312
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
KVD PHARMA INC
Original Approval or Tentative Approval Date:
August 22, 2007
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
RANITIDINE HYDROCHLORIDE
RANITIDINE HYDROCHLORIDE
15MG/ML
SOLUTION; ORAL
Tentative Approval
No
None
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