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Data / Drug companies / Concord Biotech Limited

Concord Biotech Limited: 44 products in the FDA NDC directory, labeler code 68254

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

Concord Biotech Limited (labeler code 68254) lists 44 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 33 bulk ingredients, 11 prescription drugs. Its main marketing category is bulk ingredients. The newest product started marketing on October 1, 2026.

The request: Watch Concord Biotech Limited (FDA labeler code 68254): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
68254
Products in commercial distribution
44
Packages
66
Finished drugs by generic name
5
Prescription products
11
Over the counter products
0
Flagged as original packager
9 of 9 products that carry the flag
Started marketing in the last 12 months
3
Earliest marketing start
January 1, 2006
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients3375%
Generic drugs (ANDA)1125%

Products by type

TypeProductsShare
Bulk ingredients3375%
Prescription drugs1125%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Powder3375%
Capsule49.1%
Tablet, film coated49.1%
Tablet, delayed release24.5%
Tablet12.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tofacitinib citrate68254-5012Tablet, film coatedGeneric drugs (ANDA)October 1, 2026
Tofacitinib citrate68254-5011Tablet, film coatedGeneric drugs (ANDA)October 1, 2026
Endoxifen citrate68254-0024PowderBulk ingredientsJanuary 5, 2026
Teriflunomide68254-5013Tablet, film coatedGeneric drugs (ANDA)July 7, 2025
Teriflunomide68254-5010Tablet, film coatedGeneric drugs (ANDA)July 7, 2025
Polymyxin b sulfate68254-2507PowderBulk ingredientsOctober 8, 2024
Voclosporin68254-0023PowderBulk ingredientsJanuary 1, 2024
Fidaxomicin68254-0022PowderBulk ingredientsDecember 1, 2023
Mycophenolate mofetil68254-2508PowderBulk ingredientsNovember 9, 2023
Nystatin68254-2506PowderBulk ingredientsOctober 8, 2023
Mycophenolate mofetil68254-5003TabletGeneric drugs (ANDA)December 21, 2020
Tacrolimus68254-5006CapsuleGeneric drugs (ANDA)November 23, 2020
Tacrolimus68254-5005CapsuleGeneric drugs (ANDA)November 23, 2020
Tacrolimus68254-5004CapsuleGeneric drugs (ANDA)November 23, 2020
Mycophenolic acid68254-5002Tablet, delayed releaseGeneric drugs (ANDA)December 13, 2019
Mycophenolic acid68254-5001Tablet, delayed releaseGeneric drugs (ANDA)December 13, 2019
Midostaurin68254-0021PowderBulk ingredientsNovember 1, 2019
Tacrolimus68254-0020PowderBulk ingredientsOctober 16, 2019
Mycophenolate mofetil68254-5000CapsuleGeneric drugs (ANDA)October 1, 2019
Dactinomycin68254-0017PowderBulk ingredientsMay 16, 2016
Mitomycin68254-0016PowderBulk ingredientsMay 16, 2016
Pimecrolimus68254-0014PowderBulk ingredientsAugust 1, 2014
Mycophenolate mofetil68254-0015PowderBulk ingredientsJuly 1, 2014
Anidulafungin68254-0013PowderBulk ingredientsJuly 1, 2014
Micafungin sodium68254-0012PowderBulk ingredientsMay 13, 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.