Data / Drug companies / Oxycodone hydrochloride and acetaminophen
Oxycodone hydrochloride and acetaminophen: 6 companies and 14 products in the FDA NDC directory
Oxycodone hydrochloride and acetaminophen is listed in the FDA National Drug Code Directory by 6 companies, with 14 products in commercial distribution. 14 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; solution, and the newest product started marketing on June 9, 2026.
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- Companies listing it
- 6
- Products
- 14
- Generic (ANDA) products
- 14 (100.0%)
- Application numbers
- 5
- Controlled substance schedule
- Schedule II
- Routes
- Oral
- Brand names
- Percocet, Oxycodone and Acetaminophen, Prolate
- openFDA record search
- api.fda.gov
Companies that list oxycodone hydrochloride and acetaminophen
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Elite Laboratories, Inc. | 3 | tablet | Generic drugs (ANDA) | December 4, 2017 |
| SpecGx LLC | 3 | tablet | Generic drugs (ANDA) | November 30, 2001 |
| SpecGx LLC | 3 | tablet | Generic drugs (ANDA) | June 30, 2004 |
| St. Mary's Medical Park Pharmacy | 3 | tablet | Generic drugs (ANDA) | June 9, 2026 |
| FH2 Pharma LLC | 1 | solution | Generic drugs (ANDA) | March 1, 2020 |
| Forte Bio-Pharma LLC | 1 | solution | Generic drugs (ANDA) | March 1, 2020 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 12 | 85.7% |
| Solution | 2 | 14.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 14 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Opioid Agonist | 14 |
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.