Skip to the page

Data / Drug companies / BioSpectra

BioSpectra: 10 products in the FDA NDC directory, labeler code 64173

BioSpectra (labeler code 64173) 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 June 22, 2026.

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
64173
Products in commercial distribution
10
Packages
10
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
3
Earliest marketing start
February 10, 2016
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
Crystal10100%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Tromethamine64173-204CrystalBulk ingredientsJune 22, 2026
Tromethamine64173-204CrystalBulk ingredientsJune 22, 2026
Potassium bromide64173-203CrystalBulk ingredientsJune 19, 2026
Potassium bromide64173-203CrystalBulk ingredientsSeptember 30, 2025
Tromethamine64173-101CrystalBulk ingredientsSeptember 20, 2023
Potassium bromide64173-203CrystalBulk ingredientsOctober 27, 2022
Tromethamine64173-204CrystalBulk ingredientsJuly 22, 2022
Tromethamine64173-101CrystalBulk ingredientsJune 27, 2017
Tromethamine64173-101CrystalBulk ingredientsMay 23, 2016
Potassium bromide64173-203CrystalBulk ingredientsFebruary 10, 2016

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