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Data / Drug companies / Fresenius Kabi Austria GmbH

Fresenius Kabi Austria GmbH: 6 products in the FDA NDC directory, labeler code 18124

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

Fresenius Kabi Austria GmbH (labeler code 18124) lists 6 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 3 prescription drugs, 3 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on May 12, 2022.

The request: Watch Fresenius Kabi Austria GmbH (FDA labeler code 18124): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
18124
Products in commercial distribution
6
Packages
8
Finished drugs by generic name
2
Prescription products
3
Over the counter products
0
Flagged as original packager
2 of 2 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1995
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients350%
Generic drugs (ANDA)116.7%
Drugs for further processing116.7%
New drug applications (NDA)116.7%

Products by type

TypeProductsShare
Prescription drugs350%
Bulk ingredients350%

Drugs it lists

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

DrugProductsCompanies listing it
Lactulose118
Clevidipine11

Dosage forms

Dosage formProductsShare
Powder350%
Solution116.7%
Injection116.7%
Emulsion116.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lactulose18124-007PowderBulk ingredientsMay 12, 2022
Lactulose18124-003PowderBulk ingredientsSeptember 1, 2017
Lactulose18124-002SolutionGeneric drugs (ANDA)December 10, 2012
Hydroxyprogesterone caproate18124-016InjectionDrugs for further processingFebruary 3, 2011
Cleviprex18124-011EmulsionNew drug applications (NDA)September 15, 2008
Hetastarch18124-009PowderBulk ingredientsJanuary 1, 1995

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.