Data / Drug companies / Rumex crispus
Rumex crispus: 4 companies and 16 products in the FDA NDC directory
Rumex crispus is listed in the FDA National Drug Code Directory by 4 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; solution; injection, and the newest product started marketing on June 1, 2026.
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- Companies listing it
- 4
- Products
- 16
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 2
- Routes
- Oral, Intradermal, Subcutaneous, Percutaneous, Cutaneous
- Brand names
- Yellow Curly Dock, Dock, Yellow Pollen
- openFDA record search
- api.fda.gov
Companies that list rumex crispus
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Hahnemann Laboratories, Inc. | 9 | pellet | Unapproved homeopathic products | November 22, 2022 |
| Greer Laboratories, Inc. | 5 | solution | Biologics (BLA) | September 15, 1981 |
| Allermed Laboratories, Inc. | 1 | injection | Biologics (BLA) | March 12, 1974 |
| Total Operations Management LLC DBA:Bestmade Natural Products Micro | 1 | globule | Unapproved homeopathic products | June 1, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Pellet | 9 | 56.2% |
| Solution | 5 | 31.2% |
| Injection | 1 | 6.2% |
| Globule | 1 | 6.2% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Unapproved homeopathic products | 10 | 62.5% |
| Biologics (BLA) | 6 | 37.5% |
Pharmacologic classes
| Class | Products |
|---|---|
| Non-Standardized Pollen Allergenic Extract | 6 |
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.