Visitor Monitoring Drug Details: ZANTAC 150
 
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Drug Details

Drug Name: ZANTAC 150
FDA Application No: (NDA) 018703
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: June 9, 1983
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ZANTAC 150 RANITIDINE HYDROCHLORIDEEQ 150MG BASETABLET; ORAL Prescription No AB
ZANTAC 300 RANITIDINE HYDROCHLORIDEEQ 300MG BASETABLET; ORAL Prescription Yes AB


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On Saturday, March 30, 2019 Elisabeth Martin wrote:
 
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On Friday, June 9, 2017 Toni wrote:
 
I failed a urine screen multiple times since I started taking Zantac, I failed for methadone & cocaine, I know I haven't done those drugs it has to be Zantac, I just need some proof. This is crazy. All I take is subutex, orandestrian, Zantac & fioricet.
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