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Data / Drug companies / Janssen Pharmaceutical Sciences Unlimited Company

Janssen Pharmaceutical Sciences Unlimited Company: 22 products in the FDA NDC directory, labeler code 65267

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

Janssen Pharmaceutical Sciences Unlimited Company (labeler code 65267) lists 22 products in the FDA National Drug Code Directory. By type: 19 bulk ingredients, 3 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on August 9, 2023.

The request: Watch Janssen Pharmaceutical Sciences Unlimited Company (FDA labeler code 65267): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
65267
Products in commercial distribution
22
Packages
23
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 5, Schedule III 3
Started marketing in the last 12 months
0
Earliest marketing start
September 11, 1992
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients1986.4%
Drugs for further processing313.6%

Products by type

TypeProductsShare
Bulk ingredients1986.4%
Drugs for further processing313.6%

Dosage forms

Dosage formProductsShare
Powder1568.2%
Solution418.2%
Injection29.1%
Pellet14.5%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Talquetamab65267-901SolutionDrugs for further processingAugust 9, 2023
Teclistamab65267-897InjectionBulk ingredientsAugust 28, 2022
Esketamine65267-117PowderBulk ingredientsMarch 5, 2019
Apalutamide65267-116PowderBulk ingredientsFebruary 14, 2018
Methylphenidate hydrochloride65267-115PowderBulk ingredientsJanuary 31, 2017
Siltuximab dpc65267-903SolutionDrugs for further processingApril 23, 2014
Buprenorphine65267-203PowderBulk ingredientsApril 30, 2012
Buprenorphine hydrochloride65267-104PowderBulk ingredientsApril 30, 2012
Rilpivirine hydrochloride65267-501PowderBulk ingredientsJuly 19, 2010
Ustekinumab65267-896InjectionBulk ingredientsSeptember 28, 2009
Golimumab65267-899SolutionBulk ingredientsApril 24, 2009
Tapentadol hydrochloride65267-101PowderBulk ingredientsJanuary 22, 2009
Tapentadol hydrochloride65267-101PowderBulk ingredientsJanuary 22, 2009
Methylphenidate hydrochloride65267-114PowderBulk ingredientsDecember 19, 2008
Darunavir ethanolate65267-210PowderBulk ingredientsFebruary 25, 2008
Paliperidone65267-201PowderBulk ingredientsDecember 19, 2006
Hydromorphone hydrochloride65267-057PowderBulk ingredientsJune 29, 2006
Risperidone65267-895PowderBulk ingredientsOctober 29, 2003
Topiramate65267-103PowderBulk ingredientsSeptember 12, 2003
Infliximab65267-898SolutionBulk ingredientsAugust 24, 1998
Risperidone65267-303PowderBulk ingredientsDecember 29, 1993
Itraconazole pellets65267-900PelletDrugs for further processingSeptember 11, 1992

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.