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Data / Drug companies / Rentschler Biopharma Se

Rentschler Biopharma Se: 8 products in the FDA NDC directory, labeler code 64538

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

Rentschler Biopharma Se (labeler code 64538) lists 8 products in the FDA National Drug Code Directory. By type: 8 bulk ingredients. Its main marketing category is bulk ingredients for compounding. The newest product started marketing on May 27, 2026.

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Labeler code
64538
Products in commercial distribution
8
Packages
8
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
1
Earliest marketing start
October 23, 2014
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients for compounding562.5%
Bulk ingredients337.5%

Products by type

TypeProductsShare
Bulk ingredients8100%

Dosage forms

Dosage formProductsShare
Injection337.5%
Injection, solution337.5%
Injection, powder, lyophilized, for solution225%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Pivekimab sunirine-pvzy64538-282Injection, powder, lyophilized, for solutionBulk ingredients for compoundingMay 27, 2026
Ustekinumab-aauz64538-824InjectionBulk ingredientsFebruary 22, 2024
Bimzelx64538-780Injection, solutionBulk ingredients for compoundingOctober 17, 2023
Epcoritamab-bysp64538-002InjectionBulk ingredientsMay 19, 2023
Velmanase alfa-tycv64538-180Injection, powder, lyophilized, for solutionBulk ingredientsMarch 1, 2023
Lanadelumab-flyo64538-644Injection, solutionBulk ingredients for compoundingAugust 24, 2018
Mepsevii64538-001InjectionBulk ingredients for compoundingNovember 15, 2017
Antihemophilic factor (recombinant), porcine sequence64538-500Injection, solutionBulk ingredients for compoundingOctober 23, 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.