Product Details for: Novolin 70/30
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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
300UNITS/10ML (30UNITS/ML); 700UNITS/10ML (70UNITS/ML)
Multi-Dose Vial
351(a)
Novolin 70/30
OTC
002
Injection
Subcutaneous
90UNITS/3ML (30UNITS/ML); 210UNITS/3ML (70UNITS/ML)
Autoinjector
351(a)
Novolin 70/30
OTC
Proper Name
insulin isophane human and insulin human
insulin isophane human and insulin human
BLA Number
019991
019991
Applicant
Novo Nordisk Inc.
Novo Nordisk Inc.
Original Approval Date
June 25, 1991
June 25, 1991
Date of First Licensure