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Data / Drug companies / Evonik Corporation

Evonik Corporation: 14 products in the FDA NDC directory, labeler code 62128

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

Evonik Corporation (labeler code 62128) lists 14 products in the FDA National Drug Code Directory. By type: 14 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on December 13, 2024.

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Labeler code
62128
Products in commercial distribution
14
Packages
16
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
June 25, 1968
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients1285.7%
Export only214.3%

Products by type

TypeProductsShare
Bulk ingredients14100%

Dosage forms

Dosage formProductsShare
Powder1178.6%
Liquid214.3%
Suspension17.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Gemcitabine hydrochloride62128-0383PowderExport onlyDecember 13, 2024
Mgl-319662128-0396PowderBulk ingredientsMarch 14, 2024
Vonoprazan fumarate62128-0397PowderBulk ingredientsNovember 21, 2023
Linzagolix choline62128-0395PowderExport onlyJune 14, 2022
Baloxavir marboxil62128-0394PowderBulk ingredientsDecember 2, 2021
Lubabegron fumarate62128-0393PowderBulk ingredientsNovember 6, 2018
Alectinib hcl62128-0384PowderBulk ingredientsDecember 11, 2015
Enzalutamide62128-0388PowderBulk ingredientsSeptember 1, 2015
Duloxetine hydrochloride62128-0386PowderBulk ingredientsAugust 3, 2004
Tadalafil62128-0385PowderBulk ingredientsNovember 26, 2003
Tilmicosin aqueous62128-0389LiquidBulk ingredientsDecember 2, 1996
Ractopamine hydrochloric acid62128-0392SuspensionBulk ingredientsDecember 1, 1992
Tilmicosin62128-0390PowderBulk ingredientsMarch 2, 1992
Tylosin intermediate62128-0391LiquidBulk ingredientsJune 25, 1968

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.