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Data / Drug companies / Aurum metallicum

Aurum metallicum: 5 companies and 13 products in the FDA NDC directory

Aurum metallicum is listed in the FDA National Drug Code Directory by 5 companies, with 13 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are pellet; liquid; globule, and the newest product started marketing on June 1, 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.

Companies listing it
5
Products
13
Generic (ANDA) products
0 (0.0%)
Application numbers
0
Routes
Oral
Brand names
Aurum Met
openFDA record search
api.fda.gov

Companies that list aurum metallicum

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Hahnemann Laboratories, Inc.9pelletUnapproved homeopathic productsApril 13, 2021
Energique, Inc.1liquidUnapproved homeopathic productsAugust 16, 2016
Ohm Pharma Inc.1pelletUnapproved homeopathic productsNovember 1, 2019
Rxhomeo Private Limited D.B.A. Rxhomeo, Inc1pelletUnapproved homeopathic productsSeptember 12, 2015
Total Operations Management LLC DBA:Bestmade Natural Products Micro1globuleUnapproved homeopathic productsJune 1, 2026

Dosage forms

Dosage formProductsShare
Pellet1184.6%
Liquid17.7%
Globule17.7%

Marketing categories

Marketing categoryProductsShare
Unapproved homeopathic products13100%

Pharmacologic classes

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.