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Data / Drug companies / E.r. Squibb & Sons, L.L.C.

E.r. Squibb & Sons, L.L.C.: 51 products in the FDA NDC directory, labeler code 0003

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

E.r. Squibb & Sons, L.L.C. (labeler code 0003) lists 51 products in the FDA National Drug Code Directory, covering 19 finished drugs by generic name. By type: 51 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on August 13, 2026.

The request: Watch E.r. Squibb & Sons, L.L.C. (FDA labeler code 0003): 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
0003
Products in commercial distribution
51
Packages
73
Finished drugs by generic name
19
Prescription products
51
Over the counter products
0
Flagged as original packager
39 of 39 products that carry the flag
Started marketing in the last 12 months
2
Earliest marketing start
June 24, 2003
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)3568.6%
Biologics (BLA)1631.4%

Products by type

TypeProductsShare
Prescription drugs51100%

Drugs it lists

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

DrugProductsCompanies listing it
Dasatinib618
Apixaban68
Xanomeline and trospium chloride51
Nivolumab41
Abatacept41
Triamcinolone acetonide377
Atazanavir34
Entecavir315
Repotrectinib21
Aztreonam25
Nivolumab and hyaluronidase-nvhy21
Elotuzumab21
Iberdomide21
Ipilimumab21
Deucravacitinib11
Halcinonide13
Nivolumab and relatlimab-rmbw11
Atazanavir and cobicistat11
Belatacept11

Dosage forms

Dosage formProductsShare
Tablet713.7%
Injection713.7%
Tablet, film coated59.8%
Capsule59.8%
Injection, solution59.8%
Injection, powder, lyophilized, for solution47.8%
Kit47.8%
Injection, suspension35.9%
Capsule, coated pellets35.9%
Capsule, gelatin coated23.9%
Solution23.9%
Injection, powder, for solution23.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Kinase Inhibitor8
Programmed Death Receptor-1 Blocking Antibody7
Corticosteroid4
Factor Xa Inhibitor4
Protease Inhibitor4
Selective T Cell Costimulation Modulator4
Cholinergic Muscarinic Agonist3
Cholinergic Muscarinic Antagonist3
Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor3
Monobactam Antibacterial2
Endoglycosidase2
SLAMF7-directed Immunostimulatory Antibody2
CTLA-4-directed Blocking Antibody2
Tyrosine Kinase 2 Inhibitor1
Lymphocyte Activation Gene-3 Blocker1
Cytochrome P450 3A Inhibitor1
Selective T Cell Costimulation Blocker1

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zenbexus0003-5710CapsuleNew drug applications (NDA)August 13, 2026
Zenbexus0003-5700CapsuleNew drug applications (NDA)August 13, 2026
Eliquis0003-1028Tablet, for suspensionNew drug applications (NDA)September 15, 2025
Eliquis sprinkle0003-0898CapsuleNew drug applications (NDA)September 15, 2025
Opdivo qvantig0003-6120Injection, solutionBiologics (BLA)January 2, 2025
Opdivo qvantig0003-3120Injection, solutionBiologics (BLA)December 27, 2024
Augtyro0003-4160CapsuleNew drug applications (NDA)November 1, 2024
Cobenfy0003-5200KitNew drug applications (NDA)September 27, 2024
Cobenfy0003-5150KitNew drug applications (NDA)September 27, 2024
Cobenfy0003-1100Capsule, coated pelletsNew drug applications (NDA)September 27, 2024
Cobenfy0003-0125Capsule, coated pelletsNew drug applications (NDA)September 27, 2024
Cobenfy0003-0050Capsule, coated pelletsNew drug applications (NDA)September 27, 2024
Augtyro0003-4040CapsuleNew drug applications (NDA)December 5, 2023
Sotyktu0003-0895Tablet, film coatedNew drug applications (NDA)September 9, 2022
Opdualag0003-7125InjectionBiologics (BLA)March 18, 2022
Opdivo0003-3756InjectionBiologics (BLA)August 30, 2021
Kenalog-800003-0315Injection, suspensionNew drug applications (NDA)April 12, 2019
Opdivo0003-3734InjectionBiologics (BLA)December 8, 2017
ELIQUIS 30-Day Starter Pack0003-3765KitNew drug applications (NDA)November 29, 2017
ELIQUIS 30-Day Starter Pack0003-3764KitNew drug applications (NDA)November 29, 2017
Empliciti0003-4522Injection, powder, lyophilized, for solutionBiologics (BLA)November 30, 2015
Empliciti0003-2291Injection, powder, lyophilized, for solutionBiologics (BLA)November 30, 2015
Evotaz0003-3641TabletNew drug applications (NDA)January 29, 2015
Opdivo0003-3774InjectionBiologics (BLA)December 22, 2014
Opdivo0003-3772InjectionBiologics (BLA)December 22, 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.