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Data / Drug companies / Changzhou Pharmaceutical Factory

Changzhou Pharmaceutical Factory: 11 products in the FDA NDC directory, labeler code 55488

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

Changzhou Pharmaceutical Factory (labeler code 55488) lists 11 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 6 bulk ingredients, 5 prescription drugs. Its main marketing category is bulk ingredients. The newest product started marketing on February 1, 2026.

The request: Watch Changzhou Pharmaceutical Factory (FDA labeler code 55488): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
55488
Products in commercial distribution
11
Packages
13
Finished drugs by generic name
2
Prescription products
5
Over the counter products
0
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
3
Earliest marketing start
January 1, 1981
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients654.5%
Generic drugs (ANDA)545.5%

Products by type

TypeProductsShare
Bulk ingredients654.5%
Prescription drugs545.5%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Rivaroxaban324
Ticagrelor232

Dosage forms

Dosage formProductsShare
Powder654.5%
Tablet, film coated327.3%
Tablet218.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Rivaroxaban55488-0542Tablet, film coatedGeneric drugs (ANDA)February 1, 2026
Rivaroxaban55488-0541Tablet, film coatedGeneric drugs (ANDA)February 1, 2026
Rivaroxaban55488-0540Tablet, film coatedGeneric drugs (ANDA)February 1, 2026
Ticagrelor55488-0544TabletGeneric drugs (ANDA)October 28, 2025
Ticagrelor55488-0543TabletGeneric drugs (ANDA)October 28, 2025
Lenalidomide55488-0700PowderBulk ingredientsJanuary 1, 2021
Captopril55488-0600PowderBulk ingredientsJanuary 1, 2019
Rosuvastatin calcium55488-0320PowderBulk ingredientsJanuary 1, 2003
Hydrochlorothiazide55488-0300PowderBulk ingredientsJanuary 1, 1984
Doxycycline hyclate55488-0100PowderBulk ingredientsJanuary 1, 1984
Doxycycline55488-0200PowderBulk ingredientsJanuary 1, 1981

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.