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Data / Drug companies / Josun International Limited

Josun International Limited: 10 products in the FDA NDC directory, labeler code 51551

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

Josun International Limited (labeler code 51551) lists 10 products in the FDA National Drug Code Directory. By type: 10 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on July 18, 2026.

The request: Watch Josun International Limited (FDA labeler code 51551): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
51551
Products in commercial distribution
10
Packages
27
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
2
Earliest marketing start
July 7, 2005
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients10100%

Products by type

TypeProductsShare
Bulk ingredients10100%

Dosage forms

Dosage formProductsShare
Powder880%
Liquid220%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Neomycin sulfate51551-0313PowderBulk ingredientsJuly 18, 2026
Methyl salicylate51551-0311LiquidBulk ingredientsApril 9, 2026
Methyl salicylate51551-0310LiquidBulk ingredientsJuly 17, 2023
Camphor51551-0309PowderBulk ingredientsJune 25, 2023
Menthol51551-0308PowderBulk ingredientsMay 17, 2023
Polymyxin b sulfate51551-0306PowderBulk ingredientsMarch 15, 2018
Polymyxin b sulphate51551-0304PowderBulk ingredientsFebruary 6, 2017
Bacitracin zinc51551-0302PowderBulk ingredientsFebruary 4, 2017
Bacitracin51551-0301PowderBulk ingredientsFebruary 4, 2017
Neomycin sulfate51551-0307PowderBulk ingredientsJuly 7, 2005

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.