DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZANTAC 75
FDA Application No:
(NDA) 020745
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
BOEHRINGER INGELHEIM
Original Approval or Tentative Approval Date:
February 26, 1998
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
ZANTAC 75
RANITIDINE HYDROCHLORIDE
EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
TABLET, EFFERVESCENT; ORAL
Discontinued
No
None
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