Data / Drug companies / Orphenadrine citrate
Orphenadrine citrate: 18 companies and 20 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Orphenadrine citrate is listed in the FDA National Drug Code Directory by 18 companies, with 20 products in commercial distribution. 20 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, extended release; injection; injection, solution, and the newest product started marketing on October 15, 2025.
The request: Get every company that lists orphenadrine citrate in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.
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- Companies listing it
- 18
- Products
- 20
- Generic (ANDA) products
- 20 (100.0%)
- Application numbers
- 5
- Routes
- Oral, Intramuscular, Intravenous
- openFDA record search
- api.fda.gov
Companies that list orphenadrine citrate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Advanced Rx of Tennessee, LLC | 2 | tablet, extended release | Generic drugs (ANDA) | May 23, 2023 |
| Proficient Rx LP | 2 | tablet, extended release | Generic drugs (ANDA) | February 15, 2000 |
| A-S Medication Solutions | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| Actavis Pharma, Inc. | 1 | injection | Generic drugs (ANDA) | July 8, 2010 |
| Bryant Ranch Prepack | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| Bryant Ranch Prepack | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| Hikma Pharmaceuticals USA Inc. | 1 | injection | Generic drugs (ANDA) | April 28, 2003 |
| Lupin Pharmaceuticals,Inc. | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| Northwind Health Company, LLC | 1 | tablet, extended release | Generic drugs (ANDA) | January 30, 2024 |
| NuCare Pharmaceuticals, Inc. | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| Preferred Pharmaceuticals Inc. | 1 | tablet, extended release | Generic drugs (ANDA) | June 19, 1998 |
| Quality Care Products LLC | 1 | tablet, extended release | Generic drugs (ANDA) | February 7, 2011 |
| Redpharm Drug | 1 | tablet, extended release | Generic drugs (ANDA) | February 15, 2000 |
| Remedyrepack Inc. | 1 | tablet, extended release | Generic drugs (ANDA) | October 15, 2025 |
| Sagent Pharmaceuticals | 1 | injection, solution | Generic drugs (ANDA) | October 1, 2011 |
| Sandoz Inc | 1 | tablet, extended release | Generic drugs (ANDA) | February 15, 2000 |
| St. Mary's Medical Park Pharmacy | 1 | tablet, extended release | Generic drugs (ANDA) | October 1, 2006 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, extended release | 17 | 85% |
| Injection | 2 | 10% |
| Injection, solution | 1 | 5% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 20 | 100% |
Pharmacologic classes
| Class | Products |
|---|---|
| Muscle Relaxant | 20 |
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.