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Data / Drug companies / Pharmacia & Upjohn Company LLC

Pharmacia & Upjohn Company LLC: 142 products in the FDA NDC directory, labeler code 0009

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

Pharmacia & Upjohn Company LLC (labeler code 0009) lists 142 products in the FDA National Drug Code Directory, covering 26 finished drugs by generic name. By type: 82 prescription drugs, 57 bulk ingredients. Its main marketing category is new drug applications (NDA). The newest product started marketing on December 30, 2024.

The request: Watch Pharmacia & Upjohn Company LLC (FDA labeler code 0009): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
0009
Products in commercial distribution
142
Packages
174
Finished drugs by generic name
26
Prescription products
82
Over the counter products
0
Controlled substance products
Schedule III 11, Schedule IV 3, Schedule V 1
Flagged as original packager
74 of 74 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
3
Earliest marketing start
December 15, 1952
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)7150%
Bulk ingredients5740.1%
Biologics (BLA)64.2%
Generic drugs (ANDA)64.2%
Drugs for further processing21.4%

Products by type

TypeProductsShare
Prescription drugs8257.7%
Bulk ingredients5740.1%
Drugs for further processing21.4%
Plasma derivatives10.7%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Powder5740.1%
Injection, solution2416.9%
Injection, powder, for solution1510.6%
Tablet139.2%
Injection, suspension96.3%
Kit53.5%
Injection, powder, lyophilized, for solution53.5%
Capsule32.1%
Granule, for suspension21.4%
Ointment10.7%
Granule, for solution10.7%
Cream10.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Camptosar0009-0112Injection, solutionNew drug applications (NDA)December 30, 2024
Camptosar0009-0082Injection, solutionNew drug applications (NDA)June 24, 2024
Cleocin0009-7667SuppositoryNew drug applications (NDA)February 3, 2024
Ganaxolone0009-1005PowderBulk ingredientsOctober 25, 2023
Lincocin0009-0104Injection, solutionNew drug applications (NDA)August 18, 2023
Lincocin0009-0107Injection, solutionNew drug applications (NDA)April 18, 2023
Prostin vr pediatric0009-0215Injection, solutionNew drug applications (NDA)October 3, 2022
Obeticholic acid0009-0098PowderBulk ingredientsMay 14, 2021
Provera0009-0051TabletNew drug applications (NDA)July 20, 2020
Minoxidil0009-5056PowderBulk ingredientsJanuary 1, 2020
Cleocin Phosphate0009-4073Injection, solutionNew drug applications (NDA)November 18, 2019
Provera0009-0065TabletNew drug applications (NDA)September 3, 2019
Crisaborole0009-0211OintmentDrugs for further processingApril 1, 2019
Provera0009-0287TabletNew drug applications (NDA)November 11, 2018
Somavert0009-7200KitBiologics (BLA)October 1, 2016
Somavert0009-7199KitBiologics (BLA)October 1, 2016
Somavert0009-7188KitBiologics (BLA)October 1, 2016
Somavert0009-7168KitBiologics (BLA)October 1, 2016
Somavert0009-7166KitBiologics (BLA)October 1, 2016
Trenbolone acetate0009-0075PowderBulk ingredientsMay 24, 2016
Dexamethasone acetate0009-5010PowderBulk ingredientsMay 18, 2016
Zyvox0009-5138Tablet, film coatedNew drug applications (NDA)October 12, 2015
Methylprednisolone hemisuccinate0009-0062PowderBulk ingredientsAugust 26, 2015
Dinoprostone0009-0058PowderBulk ingredientsAugust 26, 2015
Anidulafungin0009-0043PowderBulk ingredientsAugust 26, 2015

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.