Visitor Monitoring Drug History: BETAPAR
 
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: BETAPAR
FDA Application No: (NDA) 016053
Active Ingredient(s): MEPREDNISONE
Company: SCHERING
 
Label History
 
Labels are not available on this site for BETAPAR, (NDA) 016053
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/1/1980 004Manufacturing Change or Addition  
1/26/1978 003Labeling Revision  
 
There are no Therapeutic Equivalents
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