Data / Drug companies / Purisys LLC
Purisys LLC: 9 products in the FDA NDC directory, labeler code 73548
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Purisys LLC (labeler code 73548) lists 9 products in the FDA National Drug Code Directory. By type: 9 bulk ingredients. Its main marketing category is bulk ingredients. The newest product started marketing on March 2, 2026.
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- Labeler code
- 73548
- Products in commercial distribution
- 9
- Packages
- 9
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Controlled substance products
- Schedule II 4
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- March 11, 2020
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 9 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 9 | 100% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 7 | 77.8% |
| Oil | 2 | 22.2% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Naltrexone base | 73548-1060 | Powder | Bulk ingredients | March 2, 2026 |
| Dexmethylphenidate hydrochloride | 73548-2193 | Powder | Bulk ingredients | May 1, 2025 |
| Nalmefene hydrochloride | 73548-8019 | Powder | Bulk ingredients | September 2, 2024 |
| Powdered opium | 73548-8031 | Powder | Bulk ingredients | December 1, 2023 |
| Dronabinol in sesame oil | 73548-2200 | Oil | Bulk ingredients | October 15, 2021 |
| Hydromorphone hydrochloride | 73548-0057 | Powder | Bulk ingredients | July 30, 2021 |
| Dronabinol | 73548-2358 | Oil | Bulk ingredients | March 8, 2021 |
| Cannabidiol | 73548-2155 | Powder | Bulk ingredients | March 1, 2021 |
| Nabilone | 73548-2162 | Powder | Bulk ingredients | March 11, 2020 |
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.