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Data / Drug companies / Yung Shin Pharmaceutical Ind. Co., Ltd.

Yung Shin Pharmaceutical Ind. Co., Ltd.: 12 products in the FDA NDC directory, labeler code 63126

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

Yung Shin Pharmaceutical Ind. Co., Ltd. (labeler code 63126) lists 12 products in the FDA National Drug Code Directory. By type: 12 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on October 31, 2022.

The request: Watch Yung Shin Pharmaceutical Ind. Co., Ltd. (FDA labeler code 63126): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
63126
Products in commercial distribution
12
Packages
19
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
March 23, 2009
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients12100%

Products by type

TypeProductsShare
Bulk ingredients12100%

Dosage forms

Dosage formProductsShare
Powder12100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Famotidine63126-907PowderBulk ingredientsOctober 31, 2022
Cabazitaxel63126-909PowderBulk ingredientsDecember 31, 2020
Micafungin sodium63126-908PowderBulk ingredientsSeptember 1, 2020
Cinacalcet hydrochloride63126-910PowderBulk ingredientsFebruary 4, 2020
Voriconazole63126-911PowderBulk ingredientsOctober 24, 2019
Eletriptan hydrobromide63126-904PowderBulk ingredientsSeptember 24, 2015
Omeprazole63126-905PowderBulk ingredientsJune 30, 2014
Entecavir monohydrate63126-903PowderBulk ingredientsFebruary 26, 2014
Zoledronic acid63126-906PowderBulk ingredientsDecember 26, 2012
Paclitaxel63126-902PowderBulk ingredientsDecember 26, 2012
Docetaxel trihydrate63126-901PowderBulk ingredientsDecember 26, 2012
Meclofenamate sodium63126-301PowderBulk ingredientsMarch 23, 2009

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.