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Data / Drug companies / Eli Lilly Kinsale Limited

Eli Lilly Kinsale Limited: 19 products in the FDA NDC directory, labeler code 63419

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

Eli Lilly Kinsale Limited (labeler code 63419) lists 19 products in the FDA National Drug Code Directory. By type: 19 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on December 11, 2024.

The request: Watch Eli Lilly Kinsale Limited (FDA labeler code 63419): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
63419
Products in commercial distribution
19
Packages
36
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule V 1
Started marketing in the last 12 months
0
Products with a marketing end date set
3
Earliest marketing start
October 1, 1996
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients19100%

Products by type

TypeProductsShare
Bulk ingredients19100%

Dosage forms

Dosage formProductsShare
Powder1368.4%
Liquid421.1%
Solution210.5%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Orforglipron63419-0603PowderBulk ingredientsDecember 11, 2024
Insulin efsitora alfa63419-0184LiquidBulk ingredientsOctober 4, 2024
Imlunestrant63419-0264PowderBulk ingredientsAugust 2, 2024
Selpercatinib63419-0597PowderBulk ingredientsMarch 7, 2023
Mirikizumab63419-0573LiquidBulk ingredientsAugust 12, 2022
Donanemab63419-0874LiquidBulk ingredientsMarch 16, 2022
Pirtobrutinib63419-0739PowderBulk ingredientsFebruary 1, 2022
Lasmiditan hemisuccinate63419-0580PowderBulk ingredientsNovember 15, 2020
Selpercatinib63419-0681PowderBulk ingredientsJune 1, 2020
Baricitinib63419-0552PowderBulk ingredientsApril 15, 2016
Abemaciclib63419-0578PowderBulk ingredientsMarch 15, 2016
Abemaciclib63419-0554PowderBulk ingredientsMarch 15, 2016
Ixekizumab63419-0536SolutionBulk ingredientsSeptember 1, 2015
Dulaglutide63419-0525SolutionBulk ingredientsJanuary 15, 2014
Ramucirumab63419-0535LiquidBulk ingredientsJuly 31, 2013
Atomoxetine hydrochloride63419-0440PowderBulk ingredientsOctober 30, 2008
Raloxifene hydrochloride63419-0420PowderBulk ingredientsOctober 30, 2008
Olanzapine pamoate monohydrate63419-0509PowderBulk ingredientsDecember 7, 2007
Olanzapine63419-0402PowderBulk ingredientsOctober 1, 1996

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.