Data / Drug companies / Plymouth Healthcare Products LLC
Plymouth Healthcare Products LLC: 7 products in the FDA NDC directory, labeler code 61480
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Plymouth Healthcare Products LLC (labeler code 61480) lists 7 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 4 prescription drugs, 3 over the counter drugs. Its main marketing category is unapproved homeopathic products. The newest product started marketing on December 12, 2016.
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- Labeler code
- 61480
- Products in commercial distribution
- 7
- Packages
- 7
- Finished drugs by generic name
- 3
- Prescription products
- 4
- Over the counter products
- 3
- Flagged as original packager
- 7 of 7 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- October 1, 1997
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Unapproved homeopathic products | 7 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 4 | 57.1% |
| Over the counter drugs | 3 | 42.9% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Nickel sulfate, potassium bromide, and fumaric acid | 1 | 1 |
| Potassium bromide, nickel sulfate, and zinc bromide | 1 | 1 |
| Potassium bromide, nickel sulfate, and sulfur | 1 | 1 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 57.1% |
| Tablet, chewable | 2 | 28.6% |
| Liquid | 1 | 14.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Copper Absorption Inhibitor | 4 |
| Osmotic Laxative | 2 |
| Potassium Salt | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Psoriasis | 61480-105 | Liquid | Unapproved homeopathic products | December 12, 2016 |
| Acne | 61480-145 | Tablet, chewable | Unapproved homeopathic products | May 1, 2016 |
| Eczema | 61480-125 | Tablet, chewable | Unapproved homeopathic products | May 1, 2016 |
| Acunol | 61480-137 | Tablet | Unapproved homeopathic products | April 18, 2006 |
| Psorizide Forte | 61480-255 | Tablet | Unapproved homeopathic products | November 15, 2001 |
| Eczemol | 61480-127 | Tablet | Unapproved homeopathic products | November 15, 2001 |
| Psorizide Ultra | 61480-124 | Tablet | Unapproved homeopathic products | October 1, 1997 |
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.