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) 020520
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
BOEHRINGER INGELHEIM
Original Approval or Tentative Approval Date:
December 19, 1995
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
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You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
ZANTAC 75
RANITIDINE HYDROCHLORIDE
EQ 75MG BASE
TABLET; ORAL
OTC
No
None
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