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Data / Drug companies / AstraZeneca AB

AstraZeneca AB: 39 products in the FDA NDC directory, labeler code 17228

AstraZeneca AB (labeler code 17228) lists 39 products in the FDA National Drug Code Directory. By type: 33 drugs for further processing, 6 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on November 18, 2025.

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
17228
Products in commercial distribution
39
Packages
41
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
2
Earliest marketing start
September 14, 1988
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing3384.6%
Bulk ingredients615.4%

Products by type

TypeProductsShare
Drugs for further processing3384.6%
Bulk ingredients615.4%

Dosage forms

Dosage formProductsShare
Tablet, film coated1333.3%
Tablet717.9%
Powder615.4%
Tablet, extended release410.3%
Capsule410.3%
Injection, solution37.7%
Tablet, delayed release25.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Baxdrostat17228-6002Tablet, film coatedDrugs for further processingNovember 18, 2025
Baxdrostat17228-6001Tablet, film coatedDrugs for further processingNovember 18, 2025
Selumetinib17228-0640CapsuleDrugs for further processingSeptember 10, 2025
Selumetinib17228-0635CapsuleDrugs for further processingSeptember 10, 2025
Capivasertib17228-9501Tablet, film coatedDrugs for further processingNovember 10, 2023
Capivasertib17228-9500Tablet, film coatedDrugs for further processingNovember 10, 2023
Budesonide micronised co-suspension apn17228-9700PowderBulk ingredientsMarch 9, 2023
Albuterol sulfate micronised conditioned17228-9600PowderBulk ingredientsMarch 9, 2023
Micronized glycopyrronium bromide17228-4610PowderBulk ingredientsNovember 7, 2022
Micronized glycopyrronium bromide17228-5600PowderBulk ingredientsOctober 24, 2022
Acalabrutinib17228-4512Tablet, film coatedDrugs for further processingAugust 4, 2022
Omeprazole magnesium17228-0750Tablet, delayed releaseDrugs for further processingFebruary 16, 2022
Benralizumab17228-2730Injection, solutionDrugs for further processingDecember 15, 2021
Olaparib17228-0668Tablet, film coatedDrugs for further processingAugust 5, 2020
Olaparib17228-0679Tablet, film coatedDrugs for further processingAugust 4, 2020
Dapagliflozin17228-6210Tablet, film coatedDrugs for further processingMay 5, 2020
Dapagliflozin17228-6205Tablet, film coatedDrugs for further processingMay 5, 2020
Durvalumab17228-4611Injection, solutionDrugs for further processingJanuary 1, 2020
Durvalumab17228-4500Injection, solutionDrugs for further processingJanuary 1, 2020
Osimertinib17228-1350Tablet, film coatedDrugs for further processingNovember 13, 2015
Osimertinib17228-1349Tablet, film coatedDrugs for further processingNovember 13, 2015
Ticagrelor17228-0776Tablet, film coatedDrugs for further processingJune 10, 2015
Ticagrelor17228-7777PowderBulk ingredientsFebruary 10, 2014
Candesartan cilexetil hydrochlorothiazide17228-0324TabletDrugs for further processingDecember 5, 2012
Candesartan cilexetil hydrochlorothiazide17228-0322TabletDrugs for further processingDecember 5, 2012

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