Skip to the page

Data / Drug companies / Catalent Indiana, LLC

Catalent Indiana, LLC: 29 products in the FDA NDC directory, labeler code 61434

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

Catalent Indiana, LLC (labeler code 61434) lists 29 products in the FDA National Drug Code Directory. By type: 19 prescription drugs, 9 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on January 1, 2025.

The request: Watch Catalent Indiana, LLC (FDA labeler code 61434): 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
61434
Products in commercial distribution
29
Packages
31
Finished drugs by generic name
0
Prescription products
19
Over the counter products
0
Started marketing in the last 12 months
0
Products with a marketing end date set
8
Earliest marketing start
October 16, 2014
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing2586.2%
Export only310.3%
Bulk ingredients13.4%

Products by type

TypeProductsShare
Prescription drugs1965.5%
Drugs for further processing931%
Bulk ingredients13.4%

Dosage forms

Dosage formProductsShare
Injection, solution1965.5%
Injection724.1%
Injection, powder, lyophilized, for solution26.9%
Solution13.4%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Aflibercept61434-077Injection, solutionExport onlyJanuary 1, 2025
Ravulizumab61434-076Injection, solutionDrugs for further processingJanuary 1, 2025
Nivolumab61434-075Injection, solutionDrugs for further processingJanuary 1, 2025
Aflibercept61434-074Injection, solutionDrugs for further processingJanuary 1, 2025
Aflibercept61434-073Injection, solutionDrugs for further processingJanuary 1, 2025
Odronextamab61434-072Injection, solutionExport onlyJanuary 1, 2025
Odronextamab61434-064Injection, solutionExport onlyJanuary 1, 2025
Adalimumab61434-020Injection, solutionDrugs for further processingJanuary 1, 2025
Semaglutide61434-068Injection, solutionDrugs for further processingJuly 22, 2024
Semaglutide61434-067Injection, solutionDrugs for further processingJuly 22, 2024
Imetelstat sodium61434-069Injection, powder, lyophilized, for solutionDrugs for further processingJune 24, 2024
Benralizumab61434-066Injection, solutionDrugs for further processingJune 3, 2024
Pozelimab61434-063Injection, solutionDrugs for further processingAugust 18, 2023
Aflibercept61434-062Injection, solutionDrugs for further processingAugust 18, 2023
Ansuvimab-zykl61434-071Injection, powder, lyophilized, for solutionDrugs for further processingDecember 21, 2020
Ansuvimab-zykl61434-070InjectionDrugs for further processingDecember 21, 2020
Atoltivimab, maftivimab, and odesivimab61434-052Injection, solutionDrugs for further processingOctober 14, 2020
Aflibercept61434-007Injection, solutionDrugs for further processingAugust 12, 2019
Cemiplimab61434-021InjectionDrugs for further processingSeptember 28, 2018
Lanadelumab-flyo61434-019Injection, solutionDrugs for further processingAugust 24, 2018
Epinephrine61434-041InjectionDrugs for further processingAugust 22, 2018
Epinephrine61434-040InjectionDrugs for further processingAugust 22, 2018
Diluent61434-011SolutionDrugs for further processingOctober 6, 2017
Durvalumab61434-038Injection, solutionDrugs for further processingMay 1, 2017
Durvalumab injection, solution61434-002Injection, solutionDrugs for further processingMay 1, 2017

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.