Data / Drug companies / Acetaminophen and codeine phosphate
Acetaminophen and codeine phosphate: 24 companies and 68 products in the FDA NDC directory
Acetaminophen and codeine phosphate is listed in the FDA National Drug Code Directory by 24 companies, with 68 products in commercial distribution. 68 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 4, 2026.
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- Companies listing it
- 24
- Products
- 68
- Generic (ANDA) products
- 68 (100.0%)
- Application numbers
- 8
- Controlled substance schedule
- Schedule II, Schedule III, Schedule V
- Routes
- Oral
- openFDA record search
- api.fda.gov
Companies that list acetaminophen and codeine phosphate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| NuCare Pharmaceuticals,Inc. | 9 | tablet | Generic drugs (ANDA) | May 20, 2024 |
| Bryant Ranch Prepack | 7 | tablet | Generic drugs (ANDA) | May 20, 2024 |
| Advanced Rx of Tennessee, LLC | 4 | tablet | Generic drugs (ANDA) | June 2, 2025 |
| Preferred Pharmaceuticals Inc. | 4 | tablet | Generic drugs (ANDA) | June 2, 2025 |
| Remedyrepack Inc. | 4 | tablet | Generic drugs (ANDA) | June 17, 2024 |
| A-S Medication Solutions | 3 | tablet | Generic drugs (ANDA) | May 31, 2001 |
| Aurolife Pharma, LLC | 3 | tablet | Generic drugs (ANDA) | April 15, 2013 |
| Bryant Ranch Prepack | 3 | tablet | Generic drugs (ANDA) | August 2, 2019 |
| Elite Laboratories, Inc. | 3 | tablet | Generic drugs (ANDA) | September 10, 2019 |
| Eywa Pharma Inc | 3 | tablet | Generic drugs (ANDA) | August 2, 2019 |
| SpecGx LLC | 3 | tablet | Generic drugs (ANDA) | May 31, 2001 |
| Strides Pharma Science Limited | 3 | tablet | Generic drugs (ANDA) | May 20, 2024 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | tablet | Generic drugs (ANDA) | July 6, 2011 |
| Bryant Ranch Prepack | 2 | tablet | Generic drugs (ANDA) | August 2, 2019 |
| Clinical Solutions Wholesale, LLC | 2 | tablet | Generic drugs (ANDA) | February 27, 2019 |
| Pai Holdings, LLC DBA Pai Pharma | 2 | solution | Generic drugs (ANDA) | August 21, 1981 |
| Proficient Rx LP | 2 | tablet | Generic drugs (ANDA) | January 5, 2017 |
| Proficient Rx LP | 2 | tablet | Generic drugs (ANDA) | May 20, 2024 |
| St. Mary's Medical Park Pharmacy | 2 | tablet | Generic drugs (ANDA) | May 20, 2024 |
| Asclemed USA, Inc. | 1 | tablet | Generic drugs (ANDA) | August 2, 2019 |
| Direct_Rx | 1 | tablet | Generic drugs (ANDA) | August 31, 2022 |
| Genus Lifesciences | 1 | solution | Generic drugs (ANDA) | August 10, 2023 |
| Redpharm Drug | 1 | tablet | Generic drugs (ANDA) | August 2, 2019 |
| Unit Dose Solutions, Inc. | 1 | tablet | Generic drugs (ANDA) | June 4, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 65 | 95.6% |
| Solution | 3 | 4.4% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 68 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Opioid Agonist | 68 |
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.