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Data / Drug companies / CKD Bio Corporation

CKD Bio Corporation: 14 products in the FDA NDC directory, labeler code 52972

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

CKD Bio Corporation (labeler code 52972) lists 14 products in the FDA National Drug Code Directory. By type: 11 bulk ingredients, 3 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on July 26, 2023.

The request: Watch CKD Bio Corporation (FDA labeler code 52972): 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
52972
Products in commercial distribution
14
Packages
14
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
November 19, 1996
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients1178.6%
Drugs for further processing321.4%

Products by type

TypeProductsShare
Bulk ingredients1178.6%
Drugs for further processing321.4%

Dosage forms

Dosage formProductsShare
Powder14100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Clavulanate potassium52972-0042PowderDrugs for further processingJuly 26, 2023
Vancomycin hydrochloride52972-0039PowderBulk ingredientsOctober 31, 2016
Tacrolimus52972-0040PowderBulk ingredientsSeptember 29, 2016
Rifamycin o52972-0038PowderBulk ingredientsJune 21, 2012
Mycophenolate mofetil52972-0037PowderBulk ingredientsJune 7, 2011
Rifamycin sodium52972-0036PowderBulk ingredientsApril 26, 2010
Acarbose52972-0035PowderBulk ingredientsSeptember 12, 2007
Clavulanate potassium52972-0034PowderDrugs for further processingJune 10, 2005
Clavulanate potassium52972-0033PowderDrugs for further processingJune 10, 2005
Clavulanate potassium52972-0031PowderBulk ingredientsFebruary 26, 2003
Rifampin52972-0041PowderBulk ingredientsNovember 16, 1998
Demeclocycline hydrochloride52972-0030PowderBulk ingredientsNovember 16, 1998
Rifampin52972-0026PowderBulk ingredientsNovember 16, 1998
Cyclosporine52972-0027PowderBulk ingredientsNovember 19, 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.