Visitor Monitoring Drug History: RESERPINE
 
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Label and Approval History

Drug Name: RESERPINE
FDA Application No: (NDA) 010441
Active Ingredient(s): RESERPINE
Company: EVERYLIFE
 
Label History
 
Labels are not available on this site for RESERPINE, (NDA) 010441
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/3/1980 007Distributor  
2/21/1978 006Control Supplement  
 
Therapeutic Equivalents
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