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Data / Drug companies / Patheon France S.a.s.

Patheon France S.a.s.: 44 products in the FDA NDC directory, labeler code 47049

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

Patheon France S.a.s. (labeler code 47049) lists 44 products in the FDA National Drug Code Directory. By type: 44 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on May 11, 2026.

The request: Watch Patheon France S.a.s. (FDA labeler code 47049): 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
47049
Products in commercial distribution
44
Packages
46
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
26
Earliest marketing start
December 20, 2005
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing44100%

Products by type

TypeProductsShare
Drugs for further processing44100%

Dosage forms

Dosage formProductsShare
Tablet, film coated2352.3%
Capsule920.5%
Capsule, coated pellets49.1%
Capsule, gelatin coated49.1%
Tablet24.5%
Granule, for suspension12.3%
Tablet, coated12.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Mavacamten47049-056Capsule, gelatin coatedDrugs for further processingMay 11, 2026
Mavacamten47049-055Capsule, gelatin coatedDrugs for further processingMay 11, 2026
Mavacamten47049-054Capsule, gelatin coatedDrugs for further processingMay 11, 2026
Mavacamten47049-053Capsule, gelatin coatedDrugs for further processingMay 11, 2026
Riociguat47049-048Tablet, film coatedDrugs for further processingApril 1, 2026
Riociguat47049-047Tablet, film coatedDrugs for further processingApril 1, 2026
Riociguat47049-046Tablet, film coatedDrugs for further processingApril 1, 2026
Riociguat47049-045Tablet, film coatedDrugs for further processingApril 1, 2026
Riociguat47049-044Tablet, film coatedDrugs for further processingApril 1, 2026
Ponesimod47049-071Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-070Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-069Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-068Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-067Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-066Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-065Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-064Tablet, film coatedDrugs for further processingJanuary 1, 2026
Ponesimod47049-063Tablet, film coatedDrugs for further processingJanuary 1, 2026
Abiraterone acetate47049-062TabletDrugs for further processingJanuary 1, 2026
Abiraterone acetate47049-061TabletDrugs for further processingJanuary 1, 2026
Niraparib tosylate monohydrate and abiraterone acetate47049-060Tablet, film coatedDrugs for further processingJanuary 1, 2026
Niraparib tosylate monohydrate and abiraterone acetate47049-059Tablet, film coatedDrugs for further processingJanuary 1, 2026
Arimoclomol citrate47049-052CapsuleDrugs for further processingDecember 5, 2025
Arimoclomol citrate47049-051CapsuleDrugs for further processingDecember 5, 2025
Arimoclomol citrate47049-050CapsuleDrugs for further processingDecember 5, 2025

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.