Data / Drug companies / Organon LLC
Organon LLC: 67 products in the FDA NDC directory, labeler code 78206
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Organon LLC (labeler code 78206) lists 67 products in the FDA National Drug Code Directory, covering 31 finished drugs by generic name. By type: 67 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on December 1, 2025.
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- Labeler code
- 78206
- Products in commercial distribution
- 67
- Packages
- 91
- Finished drugs by generic name
- 31
- Prescription products
- 67
- Over the counter products
- 0
- Flagged as original packager
- 60 of 60 products that carry the flag
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- April 21, 2017
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 50 | 74.6% |
| Biologics (BLA) | 17 | 25.4% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 67 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Mometasone furoate | 5 | 23 |
| Mirtazapine | 5 | 42 |
| Adalimumab-bwwd | 5 | 3 |
| Montelukast sodium | 4 | 31 |
| Ezetimibe and simvastatin | 4 | 8 |
| Simvastatin | 3 | 32 |
| Tocilizumab | 3 | 4 |
| Mometasone furoate and formoterol fumarate dihydrate | 3 | 1 |
| Follitropin | 3 | 2 |
| Losartan potassium | 3 | 43 |
| Losartan potassium and hydrochlorothiazide | 3 | 31 |
| Alendronate sodium and cholecalciferol | 2 | 1 |
| Denosumab | 2 | 5 |
| Rizatriptan benzoate | 2 | 25 |
| Desloratadine | 2 | 11 |
| Carbidopa and levodopa | 2 | 41 |
| Finasteride | 2 | 31 |
| Desloratadine and pseudoephedrine sulfate | 1 | 1 |
| Ganirelix acetate | 1 | 10 |
| Etonogestrel | 1 | 1 |
| Ezetimibe | 1 | 26 |
| Copper | 1 | 4 |
| Betamethasone acetate and betamethasone sodium phosphate | 1 | 2 |
| Infliximab | 1 | 2 |
| Clindamycin phosphate | 1 | 31 |
| Betamethasone dipropionate | 1 | 27 |
| Ontruzant | 1 | 1 |
| Alendronate sodium | 1 | 16 |
| Trastuzumab | 1 | 4 |
| Choriogonadotropin alfa | 1 | 3 |
| Etonogestrel and ethinyl estradiol | 1 | 6 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 16 | 23.9% |
| Tablet | 11 | 16.4% |
| Injection, solution | 6 | 9% |
| Aerosol | 6 | 9% |
| Solution | 5 | 7.5% |
| Tablet, orally disintegrating | 4 | 6% |
| Injection | 3 | 4.5% |
| Tablet, chewable | 2 | 3% |
| Injection, powder, lyophilized, for solution | 2 | 3% |
| Kit | 2 | 3% |
| Inhalant | 2 | 3% |
| Tablet, extended release | 1 | 1.5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Miudella | 78206-210 | Intrauterine device | New drug applications (NDA) | December 1, 2025 |
| Bilprevda | 78206-195 | Injection, solution | Biologics (BLA) | September 11, 2025 |
| Bildyos | 78206-193 | Injection, solution | Biologics (BLA) | September 11, 2025 |
| Tofidence | 78206-202 | Injection | Biologics (BLA) | July 3, 2025 |
| Tofidence | 78206-201 | Injection | Biologics (BLA) | July 3, 2025 |
| Tofidence | 78206-200 | Injection | Biologics (BLA) | July 3, 2025 |
| Sinemet | 78206-190 | Tablet | New drug applications (NDA) | February 28, 2025 |
| Xaciato | 78206-189 | Gel | New drug applications (NDA) | October 13, 2023 |
| Follistim AQ | 78206-131 | Injection, solution | Biologics (BLA) | July 24, 2023 |
| Follistim AQ | 78206-130 | Injection, solution | Biologics (BLA) | July 24, 2023 |
| Follistim AQ | 78206-129 | Injection, solution | Biologics (BLA) | July 24, 2023 |
| Hadlima | 78206-187 | Solution | Biologics (BLA) | July 1, 2023 |
| Hadlima | 78206-186 | Solution | Biologics (BLA) | July 1, 2023 |
| Hadlima | 78206-185 | Solution | Biologics (BLA) | July 1, 2023 |
| Hadlima | 78206-184 | Solution | Biologics (BLA) | July 1, 2023 |
| Hadlima | 78206-183 | Solution | Biologics (BLA) | July 1, 2023 |
| Pregnyl | 78206-150 | Kit | Biologics (BLA) | June 2, 2023 |
| Clarinex | 78206-188 | Tablet, film coated | New drug applications (NDA) | August 23, 2022 |
| Zocor | 78206-182 | Tablet, film coated | New drug applications (NDA) | June 1, 2021 |
| Zocor | 78206-181 | Tablet, film coated | New drug applications (NDA) | June 1, 2021 |
| Zocor | 78206-180 | Tablet, film coated | New drug applications (NDA) | June 1, 2021 |
| Zetia | 78206-178 | Tablet | New drug applications (NDA) | June 1, 2021 |
| Vytorin | 78206-177 | Tablet | New drug applications (NDA) | June 1, 2021 |
| Vytorin | 78206-176 | Tablet | New drug applications (NDA) | June 1, 2021 |
| Vytorin | 78206-175 | Tablet | New drug applications (NDA) | June 1, 2021 |
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.