Data / Drug companies / Mercurius solubilis
Mercurius solubilis: 7 companies and 16 products in the FDA NDC directory
Mercurius solubilis is listed in the FDA National Drug Code Directory by 7 companies, with 16 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; globule; liquid, and the newest product started marketing on June 1, 2026.
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- Companies listing it
- 7
- Products
- 16
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 0
- Routes
- Oral, Sublingual
- openFDA record search
- api.fda.gov
Companies that list mercurius solubilis
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Boiron | 9 | pellet | Unapproved homeopathic products | March 3, 1983 |
| Sevene USA | 2 | pellet | Unapproved homeopathic products | November 30, 2011 |
| BM Private Limited | 1 | globule | Unapproved homeopathic products | January 1, 2015 |
| Newton Laboratories, Inc. | 1 | liquid | Unapproved homeopathic products | April 11, 2023 |
| Professional Complementary Health Formulas | 1 | liquid | Unapproved homeopathic products | August 15, 1984 |
| Rxhomeo Private Limited D.B.A. Rxhomeo, Inc | 1 | pellet | Unapproved homeopathic products | September 10, 2015 |
| Total Operations Management LLC DBA:Bestmade Natural Products Micro | 1 | globule | Unapproved homeopathic products | June 1, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Pellet | 12 | 75% |
| Globule | 2 | 12.5% |
| Liquid | 2 | 12.5% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Unapproved homeopathic products | 16 | 100% |
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.