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Data / Drug companies / Nantong Chanyoo Pharmatech Co., Ltd

Nantong Chanyoo Pharmatech Co., Ltd: 13 products in the FDA NDC directory, labeler code 69218

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

Nantong Chanyoo Pharmatech Co., Ltd (labeler code 69218) lists 13 products in the FDA National Drug Code Directory. By type: 13 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on July 15, 2026.

The request: Watch Nantong Chanyoo Pharmatech Co., Ltd (FDA labeler code 69218): 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
69218
Products in commercial distribution
13
Packages
13
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
3
Earliest marketing start
January 1, 2015
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients13100%

Products by type

TypeProductsShare
Bulk ingredients13100%

Dosage forms

Dosage formProductsShare
Powder13100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Sacubitril valsartan sodium69218-1003PowderBulk ingredientsJuly 15, 2026
Eltrombopag olamine69218-1004PowderBulk ingredientsJuly 1, 2026
Doxycycline69218-1002PowderBulk ingredientsDecember 1, 2025
Ticagrelor69218-1001PowderBulk ingredientsApril 30, 2025
Ticagrelor69218-1000PowderBulk ingredientsApril 30, 2025
Apixaban69218-0900PowderBulk ingredientsDecember 30, 2022
Ezetimibe69218-0800PowderBulk ingredientsJanuary 1, 2021
Tofacitinib citrate69218-0700PowderBulk ingredientsJanuary 1, 2021
Rosuvastatin calcium69218-0600PowderBulk ingredientsJanuary 1, 2021
Rivaroxaban69218-0500PowderBulk ingredientsJanuary 1, 2020
Ezetimibe69218-0400PowderBulk ingredientsJanuary 1, 2018
Pregabalin69218-0300PowderBulk ingredientsJanuary 1, 2018
Rosuvastatin calcium69218-0100PowderBulk ingredientsJanuary 1, 2015

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.