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Data / Drug companies / Patheon Inc.

Patheon Inc.: 55 products in the FDA NDC directory, labeler code 66406

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

Patheon Inc. (labeler code 66406) lists 55 products in the FDA National Drug Code Directory. By type: 55 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on May 15, 2026.

The request: Watch Patheon Inc. (FDA labeler code 66406): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
66406
Products in commercial distribution
55
Packages
66
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
3
Products with a marketing end date set
2
Earliest marketing start
December 15, 1952
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing55100%

Products by type

TypeProductsShare
Drugs for further processing55100%

Dosage forms

Dosage formProductsShare
Tablet, film coated1629.1%
Tablet1527.3%
Capsule, gelatin coated59.1%
Tablet, extended release35.5%
Solution35.5%
Tablet, coated35.5%
Tablet, film coated, extended release35.5%
Capsule23.6%
Tablet, multilayer, extended release23.6%
Powder11.8%
Suspension11.8%
Tablet, for suspension11.8%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tetraferric tricitrate decahydrate66406-0280Tablet, coatedDrugs for further processingMay 15, 2026
Dextromethorphan hydrobromide and bupropion hydrochloride66406-0467Tablet, multilayer, extended releaseDrugs for further processingMay 1, 2026
Sirolimus solution66406-0465SolutionDrugs for further processingMarch 11, 2026
Acoramidis hydrochloride66406-0460Tablet, film coatedDrugs for further processingSeptember 15, 2025
Famotidine66406-0446Tablet, film coatedDrugs for further processingMarch 11, 2024
Emtricitabine and tenofovir disoproxil fumarate66406-0464Tablet, film coatedDrugs for further processingJanuary 13, 2023
Emtricitabine and tenofovir disoproxil fumarate66406-0463Tablet, film coatedDrugs for further processingJanuary 13, 2023
Emtricitabine and tenofovir disoproxil fumarate66406-0462Tablet, film coatedDrugs for further processingJanuary 13, 2023
Voxelotor66406-0442Tablet, film coatedDrugs for further processingOctober 14, 2022
Sodium phenylbutyrate and ursodoxicoltaurine66406-0338PowderDrugs for further processingSeptember 29, 2022
Dextromethorphan hydrobromide and bupropion hydrochloride66406-0336Tablet, multilayer, extended releaseDrugs for further processingAugust 18, 2022
Molnupiravir66406-0332CapsuleDrugs for further processingDecember 23, 2021
Voxelotor66406-0333Tablet, for suspensionDrugs for further processingDecember 17, 2021
Oteseconazole66406-0334Capsule, gelatin coatedDrugs for further processingNovember 5, 2021
Lumateperone66406-0300CapsuleDrugs for further processingFebruary 1, 2020
Voxelotor66406-0301Tablet, film coatedDrugs for further processingNovember 25, 2019
Bictegravir sodium, emtricitabine, and tenofovir alafenamide fumarate66406-0273TabletDrugs for further processingFebruary 7, 2018
Atazanavir sulfate and cobicistat66406-0289TabletDrugs for further processingJanuary 29, 2015
Tedizolid phosphate66406-0206Tablet, coatedDrugs for further processingJune 20, 2014
Eslicarbazepine acetate66406-0327TabletDrugs for further processingApril 7, 2014
Eslicarbazepine acetate66406-0222TabletDrugs for further processingApril 7, 2014
Eslicarbazepine acetate66406-0204TabletDrugs for further processingApril 7, 2014
Eslicarbazepine acetate66406-0203TabletDrugs for further processingApril 7, 2014
Apremilast66406-0242Tablet, film coatedDrugs for further processingMarch 25, 2014
Apremilast66406-0241Tablet, film coatedDrugs for further processingMarch 25, 2014

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.