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Data / Drug companies / Novo Nordisk Pharma, Inc.

Novo Nordisk Pharma, Inc.: 8 products in the FDA NDC directory, labeler code 73070

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Novo Nordisk Pharma, Inc. (labeler code 73070) lists 8 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 8 prescription drugs. Its main marketing category is biologics (BLA). The newest product started marketing on July 1, 2022.

The request: Watch Novo Nordisk Pharma, Inc. (FDA labeler code 73070): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
73070
Products in commercial distribution
8
Packages
8
Finished drugs by generic name
2
Prescription products
8
Over the counter products
0
Flagged as original packager
8 of 8 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
8
Earliest marketing start
August 27, 2001
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Biologics (BLA)8100%

Products by type

TypeProductsShare
Prescription drugs8100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Insulin aspart54
Insulin degludec33

Dosage forms

Dosage formProductsShare
Injection, solution675%
Injection, suspension225%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Insulin Analog8

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Insulin Degludec73070-503Injection, solutionBiologics (BLA)July 1, 2022
Insulin Degludec73070-403Injection, solutionBiologics (BLA)July 1, 2022
Insulin Degludec73070-400Injection, solutionBiologics (BLA)July 1, 2022
Insulin Aspart73070-103Injection, solutionBiologics (BLA)January 22, 2003
Insulin Aspart Protamine and Insulin Aspart Mix 70/3073070-203Injection, suspensionBiologics (BLA)September 11, 2002
Insulin Aspart Protamine and Insulin Aspart Mix 70/3073070-200Injection, suspensionBiologics (BLA)November 1, 2001
Insulin Aspart73070-102Injection, solutionBiologics (BLA)August 27, 2001
Insulin Aspart73070-100Injection, solutionBiologics (BLA)August 27, 2001

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.