Visitor Monitoring Drug Details: ULTRALENTE
 
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Drug Details

Drug Name: ULTRALENTE
FDA Application No: (NDA) 018385
Active Ingredient(s): INSULIN ZINC SUSP EXTENDED PURIFIED BEEF
Company: NOVO NORDISK INC
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ULTRALENTE INSULIN ZINC SUSP EXTENDED PURIFIED BEEF100 UNITS/MLINJECTABLE; INJECTION Discontinued No None


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