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Data / Drug companies / Patheon Pharmaceuticals Inc.

Patheon Pharmaceuticals Inc.: 41 products in the FDA NDC directory, labeler code 67651

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

Patheon Pharmaceuticals Inc. (labeler code 67651) lists 41 products in the FDA National Drug Code Directory. By type: 41 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on July 13, 2026.

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Labeler code
67651
Products in commercial distribution
41
Packages
46
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 4, Schedule IV 4
Started marketing in the last 12 months
1
Products with a marketing end date set
1
Earliest marketing start
August 21, 2009
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing41100%

Products by type

TypeProductsShare
Drugs for further processing41100%

Dosage forms

Dosage formProductsShare
Tablet, film coated1741.5%
Capsule1024.4%
Tablet512.2%
Tablet, film coated, extended release24.9%
Tablet, chewable24.9%
Tablet, delayed release24.9%
Granule, for suspension12.4%
Powder, for solution12.4%
Tablet, coated12.4%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Doravirine, islatravir67651-0416Tablet, film coatedDrugs for further processingJuly 13, 2026
Elexacaftor, tezacaftor, and ivacaftor67651-0405Tablet, film coatedDrugs for further processingAugust 13, 2024
Vanzacaftor, tezacaftor, and deutivacaftor67651-0396Tablet, film coatedDrugs for further processingAugust 9, 2024
Vanzacaftor, tezacaftor, and deutivacaftor67651-0397Tablet, film coatedDrugs for further processingAugust 4, 2024
Elexacaftor, tezacaftor, and ivacaftor67651-0404Tablet, film coatedDrugs for further processingApril 26, 2024
Lisdexamfetamine dimesylate67651-0388CapsuleDrugs for further processingFebruary 19, 2024
Lisdexamfetamine dimesylate67651-0387CapsuleDrugs for further processingFebruary 19, 2024
Lisdexamfetamine dimesylate67651-0386CapsuleDrugs for further processingFebruary 19, 2024
Suvorexant67651-0385Tablet, film coatedDrugs for further processingJanuary 20, 2024
Suvorexant67651-0384Tablet, film coatedDrugs for further processingJanuary 20, 2024
Suvorexant67651-0383Tablet, film coatedDrugs for further processingJanuary 20, 2024
Suvorexant67651-0382Tablet, film coatedDrugs for further processingJanuary 20, 2024
Tenapanor67651-0381Tablet, film coatedDrugs for further processingOctober 17, 2023
Tenapanor67651-0380Tablet, film coatedDrugs for further processingOctober 17, 2023
Tenapanor67651-0393Tablet, film coatedDrugs for further processingSeptember 25, 2023
Pitolisant hydrochloride67651-0406Tablet, film coatedDrugs for further processingAugust 27, 2023
Omadacycline67651-0375Tablet, film coatedDrugs for further processingSeptember 27, 2022
Molnupiravir67651-0365CapsuleDrugs for further processingDecember 23, 2021
Avacopan67651-0364CapsuleDrugs for further processingOctober 18, 2021
Avacopan67651-0363CapsuleDrugs for further processingOctober 18, 2021
Selumetinib67651-0344CapsuleDrugs for further processingApril 16, 2020
Selumetinib67651-0343CapsuleDrugs for further processingApril 16, 2020
Tenapanor hydrochloride67651-0335TabletDrugs for further processingSeptember 12, 2019
Amifampridine phosphate67651-0328TabletDrugs for further processingJanuary 7, 2019
Prucalopride succinate67651-0331Tablet, film coatedDrugs for further processingDecember 14, 2018

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.