Skip to the page

Data / Drug companies / Catalent U.k. Swindon Zydis Limited

Catalent U.k. Swindon Zydis Limited: 21 products in the FDA NDC directory, labeler code 62938

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

Catalent U.k. Swindon Zydis Limited (labeler code 62938) lists 21 products in the FDA National Drug Code Directory. By type: 21 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on February 1, 2023.

The request: Watch Catalent U.k. Swindon Zydis Limited (FDA labeler code 62938): 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
62938
Products in commercial distribution
21
Packages
32
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
June 1, 2000
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing21100%

Products by type

TypeProductsShare
Drugs for further processing21100%

Dosage forms

Dosage formProductsShare
Tablet, orally disintegrating1257.1%
Tablet942.9%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Fingolimod lauryl sulfate62938-0044Tablet, orally disintegratingDrugs for further processingFebruary 1, 2023
Fingolimod lauryl sulfate62938-0043Tablet, orally disintegratingDrugs for further processingFebruary 1, 2023
Glycopyrrolate62938-0042Tablet, orally disintegratingDrugs for further processingFebruary 1, 2022
Rimegepant sulfate62938-0037Tablet, orally disintegratingDrugs for further processingMarch 5, 2020
Asenapine maleate62938-0041TabletDrugs for further processingFebruary 24, 2020
Asenapine maleate62938-0040TabletDrugs for further processingFebruary 24, 2020
Asenaprine maleate62938-0039TabletDrugs for further processingFebruary 24, 2020
Rizatriptan62938-0046Tablet, orally disintegratingDrugs for further processingJune 22, 2019
Odactra62938-0036TabletDrugs for further processingJuly 3, 2017
Asenaprine maleate62938-0035TabletDrugs for further processingDecember 30, 2014
Asenapine maleate62938-0045TabletDrugs for further processingDecember 1, 2014
Short ragweed pollen allergen extract62938-0028TabletDrugs for further processingApril 17, 2014
Timothy grass pollen allergen extract62938-0027TabletDrugs for further processingApril 11, 2014
Asenapine maleate62938-0016TabletDrugs for further processingSeptember 30, 2013
Loratadine62938-0004Tablet, orally disintegratingDrugs for further processingDecember 12, 2006
Selegiline hydrochloride62938-0029Tablet, orally disintegratingDrugs for further processingJune 14, 2006
Loratadine62938-0005Tablet, orally disintegratingDrugs for further processingNovember 27, 2002
Olanzapine62938-0034Tablet, orally disintegratingDrugs for further processingSeptember 1, 2001
Olanzapine62938-0033Tablet, orally disintegratingDrugs for further processingSeptember 1, 2001
Olanzapine62938-0032Tablet, orally disintegratingDrugs for further processingJune 1, 2000
Olanzapine62938-0030Tablet, orally disintegratingDrugs for further processingJune 1, 2000

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.