Skip to the page

Data / Drug companies / Organon Pharma (uk) Limited

Organon Pharma (uk) Limited: 21 products in the FDA NDC directory, labeler code 60312

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

Organon Pharma (uk) Limited (labeler code 60312) 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 October 16, 2006.

The request: Watch Organon Pharma (uk) Limited (FDA labeler code 60312): 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
60312
Products in commercial distribution
21
Packages
21
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
December 23, 1991
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, film coated1257.1%
Tablet733.3%
Tablet, chewable29.5%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sitagliptin phosphate60312-0109TabletDrugs for further processingOctober 16, 2006
Sitagliptin phosphate60312-0108TabletDrugs for further processingOctober 16, 2006
Sitagliptin phosphate60312-0107TabletDrugs for further processingOctober 16, 2006
Ezetimibe and simvastatin60312-0314TabletDrugs for further processingJuly 23, 2004
Ezetimibe and simvastatin60312-0313TabletDrugs for further processingJuly 23, 2004
Ezetimibe and simvastatin60312-0312TabletDrugs for further processingJuly 23, 2004
Ezetimibe and simvastatin60312-0311TabletDrugs for further processingJuly 23, 2004
Montelukast sodium60312-0711Tablet, chewableDrugs for further processingFebruary 20, 1998
Montelukast sodium60312-0275Tablet, chewableDrugs for further processingFebruary 20, 1998
Montelukast sodium60312-0117Tablet, film coatedDrugs for further processingFebruary 20, 1998
Mirtazapine60312-0096Tablet, film coatedDrugs for further processingJune 14, 1996
Mirtazapine60312-0095Tablet, film coatedDrugs for further processingJune 14, 1996
Losartan potassium and hydrochlorothiazide60312-0747Tablet, film coatedDrugs for further processingApril 28, 1995
Losartan potassium and hydrochlorothiazide60312-0745Tablet, film coatedDrugs for further processingApril 28, 1995
Losartan potassium and hydrochlorothiazide60312-0717Tablet, film coatedDrugs for further processingApril 28, 1995
Losartan potassium60312-0960Tablet, film coatedDrugs for further processingApril 14, 1995
Losartan potassium60312-0952Tablet, film coatedDrugs for further processingApril 14, 1995
Losartan potassium60312-0951Tablet, film coatedDrugs for further processingApril 14, 1995
Simvastatin60312-0749Tablet, film coatedDrugs for further processingDecember 23, 1991
Simvastatin60312-0740Tablet, film coatedDrugs for further processingDecember 23, 1991
Simvastatin60312-0735Tablet, film coatedDrugs for further processingDecember 23, 1991

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.