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Purple Book
Database of Licensed Biological Products

Product Details for: Novolog
Product Label Grayed out Product Label links indicate that there is no product label available for the product.

Product NumberDosage FormRoute of AdministrationStrengthProduct PresentationLicense TypeProprietary NameMarketing Status
001Injection Intravenous, Subcutaneous 1,000UNITS/10ML (100UNITS/ML)Multi-Dose Vial351(a)NovologRx
002Injection Subcutaneous300UNITS/3ML (100UNITS/ML)Multi-Dose Cartridge351(a)NovologRx
003Injection Subcutaneous300UNITS/3ML (100UNITS/ML)Autoinjector351(a)NovologRx
004Injection Subcutaneous300UNITS/3ML (100UNITS/ML)Autoinjector351(a)NovologDisc
005Injection Subcutaneous300UNITS/3ML (100UNITS/ML)Autoinjector351(a)NovologDisc

Proper Name
insulin aspart

BLA Number
020986

Applicant
Novo Nordisk Inc.

Original Approval Date
June 7, 2000

Date of First Licensure