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Data / Drug companies / Miyoshi America, Inc.

Miyoshi America, Inc.: 23 products in the FDA NDC directory, labeler code 76002

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

Miyoshi America, Inc. (labeler code 76002) lists 23 products in the FDA National Drug Code Directory. By type: 23 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on September 1, 2025.

The request: Watch Miyoshi America, Inc. (FDA labeler code 76002): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
76002
Products in commercial distribution
23
Packages
25
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
May 11, 2000
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing23100%

Products by type

TypeProductsShare
Drugs for further processing23100%

Dosage forms

Dosage formProductsShare
Powder1565.2%
Powder, for solution313%
Solution313%
Liquid14.3%
Solution, concentrate14.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zinc oxide76002-0800PowderDrugs for further processingSeptember 1, 2025
Zinc oxide76002-0700PowderDrugs for further processingSeptember 1, 2025
Zinc oxide76002-0600PowderDrugs for further processingDecember 2, 2024
Zinc oxide76002-0500LiquidDrugs for further processingSeptember 4, 2024
Zinc oxide76002-0401PowderDrugs for further processingAugust 27, 2024
Zinc oxide76002-0400PowderDrugs for further processingMarch 1, 2024
Titanium dioxide76002-0300Powder, for solutionDrugs for further processingMarch 25, 2023
Titanium dioxide76002-0200Powder, for solutionDrugs for further processingAugust 1, 2022
Titanium dioxide76002-0120PowderDrugs for further processingJuly 30, 2018
Titanium dioxide76002-0130PowderDrugs for further processingJuly 20, 2018
Zinc oxide76002-0140Powder, for solutionDrugs for further processingJuly 18, 2018
Titanium dioxide76002-0110PowderDrugs for further processingJuly 18, 2018
Titanium dioxide76002-0100PowderDrugs for further processingJuly 18, 2018
Titanium dioxide76002-0055PowderDrugs for further processingSeptember 1, 2017
Titanium dioxide76002-0054PowderDrugs for further processingSeptember 1, 2017
Titanium dioxide76002-0052SolutionDrugs for further processingApril 4, 2016
Titanium dioxide76002-0051SolutionDrugs for further processingApril 4, 2016
Titanium dioxide76002-0049Solution, concentrateDrugs for further processingApril 4, 2016
Titanium dioxide76002-0048SolutionDrugs for further processingApril 4, 2016
Titanium dioxide76002-0046PowderDrugs for further processingApril 1, 2016
Titanium dioxide76002-0045PowderDrugs for further processingApril 1, 2016
Titanium dioxide76002-0017PowderDrugs for further processingApril 20, 2007
Titanium dioxide76002-0002PowderDrugs for further processingMay 11, 2000

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.