FDA Drug Application (018385) for ULTRALENTE by NOVO NORDISK INC

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Application Number018385
Product Number001
FormINJECTABLE;INJECTION
Dosage100 UNITS/ML
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameULTRALENTE
Active IngredientINSULIN ZINC SUSP EXTENDED PURIFIED BEEF



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