DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZANTAC 150
FDA Application No:
(NDA) 021698
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
BOEHRINGER INGELHEIM
Original Approval or Tentative Approval Date:
August 31, 2004
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
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 150
RANITIDINE HYDROCHLORIDE
EQ 150MG BASE
TABLET; ORAL
OTC
Yes
None
ZANTAC 150
RANITIDINE HYDROCHLORIDE
EQ 150MG BASE
TABLET; ORAL
OTC
No
None
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