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Data / Drug companies / ScinoPharm Taiwan Ltd.

ScinoPharm Taiwan Ltd.: 95 products in the FDA NDC directory, labeler code 65129

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

ScinoPharm Taiwan Ltd. (labeler code 65129) lists 95 products in the FDA National Drug Code Directory. By type: 95 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on September 24, 2026.

The request: Watch ScinoPharm Taiwan Ltd. (FDA labeler code 65129): 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
65129
Products in commercial distribution
95
Packages
95
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule III 1, Schedule V 1
Started marketing in the last 12 months
2
Earliest marketing start
January 19, 2001
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients95100%

Products by type

TypeProductsShare
Bulk ingredients95100%

Dosage forms

Dosage formProductsShare
Powder9498.9%
Oil11.1%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Exemestane65129-1217PowderBulk ingredientsSeptember 24, 2026
Alectinib hydrochloride65129-1496PowderBulk ingredientsDecember 29, 2025
Mifepristone65129-2073PowderBulk ingredientsSeptember 26, 2025
Tucatinib65129-1487PowderBulk ingredientsMarch 27, 2025
Nelarabine65129-1265PowderBulk ingredientsDecember 1, 2023
Enzalutamide65129-1482PowderBulk ingredientsSeptember 1, 2023
Ibrutinib65129-1471PowderBulk ingredientsJuly 17, 2023
Cedazuridine65129-1466PowderBulk ingredientsJuly 1, 2023
Apixaban65129-1465PowderBulk ingredientsJanuary 16, 2023
Osimertinib mesylate65129-1451PowderBulk ingredientsJune 1, 2022
Sugammadex sodium65129-1418PowderBulk ingredientsJanuary 7, 2022
Ganaxolone65129-3162PowderBulk ingredientsJune 1, 2021
Tetrahydrouridine65129-3381PowderBulk ingredientsMarch 8, 2021
Forsaprepitant dimeglumine65129-1322PowderBulk ingredientsFebruary 26, 2021
Galantamine benzoate gluconate65129-2455PowderBulk ingredientsFebruary 24, 2021
Lifitegrast65129-1428PowderBulk ingredientsOctober 1, 2020
Liraglutide65129-1375PowderBulk ingredientsSeptember 30, 2020
Ivacaftor65129-1450PowderBulk ingredientsAugust 1, 2020
Elagolix sodium65129-1443PowderBulk ingredientsApril 1, 2020
Apremilast65129-1383PowderBulk ingredientsDecember 27, 2019
Premetrexed disodium65129-1430PowderBulk ingredientsJuly 4, 2019
Brexpiprazole65129-1401PowderBulk ingredientsApril 12, 2019
Teriparatide65129-1312PowderBulk ingredientsApril 12, 2019
Palbociclib65129-1394PowderBulk ingredientsJuly 16, 2018
Olaparib65129-1464PowderBulk ingredientsMay 18, 2018

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.