Visitor Monitoring Drug History: RANITIDINE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: RANITIDINE
FDA Application No: (ANDA) 075497
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: GENPHARM
 
Label History
 
Labels are not available on this site for RANITIDINE, (ANDA) 075497
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/16/2001 002Control Supplement  
10/26/2000 001Supplier Addition  
1/14/2000 000Approval Letter 
 
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