Data / Drug companies / Oxford Pharmaceuticals, LLC
Oxford Pharmaceuticals, LLC: 35 products in the FDA NDC directory, labeler code 69584
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Oxford Pharmaceuticals, LLC (labeler code 69584) lists 35 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 35 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on May 1, 2025.
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- Labeler code
- 69584
- Products in commercial distribution
- 35
- Packages
- 114
- Finished drugs by generic name
- 13
- Prescription products
- 35
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 1
- Flagged as original packager
- 31 of 31 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- August 15, 2019
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 35 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 35 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Buspirone hydrochloride | 4 | 50 |
| Sotalol hydrochloride | 4 | 25 |
| Paroxetine hydrochloride | 4 | 16 |
| Amlodipine besylate | 3 | 49 |
| Dipyridamole | 3 | 8 |
| Imipramine hydrochloride | 3 | 14 |
| Spironolactone | 3 | 45 |
| Methocarbamol | 2 | 67 |
| Glipizide | 2 | 39 |
| Primidone | 2 | 23 |
| Hydrochlorothiazide | 2 | 51 |
| Trazodone hydrochloride | 2 | 39 |
| Carisoprodol | 1 | 28 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 23 | 65.7% |
| Tablet, film coated | 9 | 25.7% |
| Tablet, coated | 3 | 8.6% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Glipizide | 69584-310 | Tablet | Generic drugs (ANDA) | May 1, 2025 |
| Glipizide | 69584-309 | Tablet | Generic drugs (ANDA) | May 1, 2025 |
| Trazodone Hydrochloride | 69584-885 | Tablet, film coated | Generic drugs (ANDA) | March 1, 2023 |
| Trazodone Hydrochloride | 69584-884 | Tablet, film coated | Generic drugs (ANDA) | January 1, 2023 |
| Paroxetine hydrochloride | 69584-674 | Tablet, film coated | Generic drugs (ANDA) | November 14, 2022 |
| Paroxetine hydrochloride | 69584-673 | Tablet, film coated | Generic drugs (ANDA) | November 14, 2022 |
| Paroxetine hydrochloride | 69584-672 | Tablet, film coated | Generic drugs (ANDA) | November 14, 2022 |
| Paroxetine hydrochloride | 69584-671 | Tablet, film coated | Generic drugs (ANDA) | November 14, 2022 |
| AMLODIPINE BESYLATE 10 mg | 69584-023 | Tablet | Generic drugs (ANDA) | October 1, 2021 |
| AMLODIPINE BESYLATE 5 mg | 69584-022 | Tablet | Generic drugs (ANDA) | October 1, 2021 |
| AMLODIPINE BESYLATE 2.5 mg | 69584-021 | Tablet | Generic drugs (ANDA) | October 1, 2021 |
| Dipyridamole | 69584-183 | Tablet, film coated | Generic drugs (ANDA) | April 15, 2021 |
| Dipyridamole | 69584-182 | Tablet, film coated | Generic drugs (ANDA) | April 15, 2021 |
| Dipyridamole | 69584-181 | Tablet, film coated | Generic drugs (ANDA) | April 15, 2021 |
| Primidone | 69584-685 | Tablet | Generic drugs (ANDA) | February 22, 2021 |
| Primidone | 69584-684 | Tablet | Generic drugs (ANDA) | February 22, 2021 |
| Spironolactone | 69584-854 | Tablet, coated | Generic drugs (ANDA) | January 4, 2021 |
| Spironolactone | 69584-853 | Tablet, coated | Generic drugs (ANDA) | January 4, 2021 |
| Spironolactone | 69584-852 | Tablet, coated | Generic drugs (ANDA) | January 4, 2021 |
| Hydrochlorothiazide | 69584-362 | Tablet | Generic drugs (ANDA) | September 25, 2020 |
| Hydrochlorothiazide | 69584-361 | Tablet | Generic drugs (ANDA) | September 25, 2020 |
| Imipramine Hydrochloride | 69584-427 | Tablet | Generic drugs (ANDA) | August 1, 2020 |
| Imipramine Hydrochloride | 69584-426 | Tablet | Generic drugs (ANDA) | August 1, 2020 |
| Imipramine Hydrochloride | 69584-425 | Tablet | Generic drugs (ANDA) | August 1, 2020 |
| Buspirone Hydrochloride | 69584-093 | Tablet | Generic drugs (ANDA) | July 27, 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.