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Data / Drug companies / Ionis Pharmaceuticals Inc.

Ionis Pharmaceuticals Inc.: 5 products in the FDA NDC directory, labeler code 71860

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

Ionis Pharmaceuticals Inc. (labeler code 71860) lists 5 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 4 prescription drugs, 1 bulk ingredients. Its main marketing category is new drug applications (NDA). The newest product started marketing on September 3, 2026.

The request: Watch Ionis Pharmaceuticals Inc. (FDA labeler code 71860): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71860
Products in commercial distribution
5
Packages
5
Finished drugs by generic name
3
Prescription products
4
Over the counter products
0
Flagged as original packager
2 of 2 products that carry the flag
Started marketing in the last 12 months
2
Earliest marketing start
December 23, 2016
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)480%
Bulk ingredients120%

Products by type

TypeProductsShare
Prescription drugs480%
Bulk ingredients120%

Drugs it lists

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

DrugProductsCompanies listing it
Olezarsen sodium21
Zilganersen11
Donidalorsen11

Dosage forms

Dosage formProductsShare
Injection, solution360%
Kit120%
Powder120%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
APOC-III-directed RNA Interaction2
Antisense Oligonucleotide2

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zanvastro71860-304KitNew drug applications (NDA)September 3, 2026
Tryngolza71860-102Injection, solutionNew drug applications (NDA)June 24, 2026
Dawnzera71860-103Injection, solutionNew drug applications (NDA)August 21, 2025
Tryngolza71860-101Injection, solutionNew drug applications (NDA)December 19, 2024
Nusinersen71860-396PowderBulk ingredientsDecember 23, 2016

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.