Product Details for: Novolin N
RETURN TO SEARCH RESULTS
PRODUCT LABEL
Grayed out Product Label links indicate that there is no product label available for the product.
Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injectable Suspension
Subcutaneous
1,000UNITS/10ML (100UNITS/ML)
Multi-Dose Vial
351(a)
Novolin N
OTC
002
Injectable Suspension
Subcutaneous
300UNITS/3ML (100UNITS/ML)
Autoinjector
351(a)
Novolin N
OTC
Proper Name
insulin isophane human
insulin isophane human
BLA Number
019959
019959
Applicant
Novo Nordisk Inc.
Novo Nordisk Inc.
Original Approval Date
July 1, 1991
July 1, 1991
Date of First Licensure