Visitor Monitoring Drug Details: RUBRAMIN PC
 
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Drug Details

Drug Name: RUBRAMIN PC
FDA Application No: (NDA) 006799
Active Ingredient(s): CYANOCOBALAMIN
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: September 29, 1950
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
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 NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
RUBRAMIN PC CYANOCOBALAMIN0.1MG/MLINJECTABLE; INJECTION Discontinued No None
RUBRAMIN PC CYANOCOBALAMIN1MG/MLINJECTABLE; INJECTION Discontinued No None
RUBRAMIN PC CYANOCOBALAMIN1MG/MLINJECTABLE; INJECTION Discontinued No None


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