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) 074552
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
MYLAN
Original Approval or Tentative Approval Date:
July 30, 1998
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
RANITIDINE HYDROCHLORIDE
RANITIDINE HYDROCHLORIDE
EQ 150MG BASE
TABLET; ORAL
Discontinued
No
None
RANITIDINE HYDROCHLORIDE
RANITIDINE HYDROCHLORIDE
EQ 300MG BASE
TABLET; ORAL
Discontinued
No
None
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