Skip to the page

Data / Drug companies / Eisai Manufacturing Ltd

Eisai Manufacturing Ltd: 11 products in the FDA NDC directory, labeler code 60510

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

Eisai Manufacturing Ltd (labeler code 60510) lists 11 products in the FDA National Drug Code Directory. By type: 11 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on April 7, 2020.

The request: Watch Eisai Manufacturing Ltd (FDA labeler code 60510): 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
60510
Products in commercial distribution
11
Packages
18
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule III 6, Schedule IV 2
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
November 25, 1996
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing11100%

Products by type

TypeProductsShare
Drugs for further processing11100%

Dosage forms

Dosage formProductsShare
Tablet654.5%
Tablet, film coated545.5%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lemborexant60510-410Tablet, film coatedDrugs for further processingApril 7, 2020
Lemborexant60510-405Tablet, film coatedDrugs for further processingApril 7, 2020
Avatrombopag maleate60510-612Tablet, film coatedDrugs for further processingMay 21, 2018
Perampanel60510-609TabletDrugs for further processingSeptember 27, 2012
Perampanel60510-608TabletDrugs for further processingSeptember 27, 2012
Perampanel60510-607TabletDrugs for further processingSeptember 27, 2012
Perampanel60510-606TabletDrugs for further processingSeptember 27, 2012
Perampanel60510-605TabletDrugs for further processingSeptember 27, 2012
Perampanel60510-604TabletDrugs for further processingSeptember 27, 2012
Donepezil hydrochloride60510-614Tablet, film coatedDrugs for further processingNovember 25, 1996
Donepezil hydrochloride60510-613Tablet, film coatedDrugs for further processingNovember 25, 1996

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.