Data / Drug companies / Paricalcitol
Paricalcitol: 13 companies and 39 products in the FDA NDC directory
Paricalcitol is listed in the FDA National Drug Code Directory by 13 companies, with 39 products in commercial distribution. 30 of the products (76.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, liquid filled; injection; capsule, and the newest product started marketing on October 9, 2018.
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- Companies listing it
- 13
- Products
- 39
- Generic (ANDA) products
- 30 (76.9%)
- Application numbers
- 11
- Routes
- Oral, Intravenous
- Brand names
- Zemplar
- openFDA record search
- api.fda.gov
Companies that list paricalcitol
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| AbbVie Inc. | 4 | injection, solution; capsule, liquid filled | New drug applications (NDA) | April 20, 2018 |
| Amneal Pharmaceuticals LLC | 4 | injection | Generic drugs (ANDA) | March 9, 2017 |
| Eugia US LLC | 4 | injection | Generic drugs (ANDA) | October 9, 2018 |
| Amneal Pharmaceuticals LLC | 3 | capsule | Generic drugs (ANDA) | January 15, 2016 |
| Aurobindo Pharma Limited | 3 | capsule, liquid filled | Generic drugs (ANDA) | January 14, 2016 |
| Bionpharma Inc. | 3 | capsule | Generic drugs (ANDA) | August 16, 2016 |
| Dr. Reddy's Laboratories Limited | 3 | capsule, liquid filled | Generic drugs (ANDA) | June 25, 2014 |
| Hikma Pharmaceuticals USA Inc. | 3 | injection | New drug applications (NDA) | November 18, 2014 |
| Marksans Pharma Limited | 3 | capsule, liquid filled | Generic drugs (ANDA) | December 31, 2016 |
| Time Cap Laboratories, Inc | 3 | capsule, liquid filled | Generic drugs (ANDA) | January 3, 2017 |
| Accord Healthcare Inc. | 2 | injection, solution | New drug applications (NDA) | March 24, 2016 |
| Bryant Ranch Prepack | 2 | capsule | Generic drugs (ANDA) | August 16, 2016 |
| Bryant Ranch Prepack | 2 | capsule | Generic drugs (ANDA) | August 16, 2016 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule, liquid filled | 14 | 35.9% |
| Injection | 11 | 28.2% |
| Capsule | 10 | 25.6% |
| Injection, solution | 4 | 10.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 30 | 76.9% |
| New drug applications (NDA) | 9 | 23.1% |
Pharmacologic classes
| Class | Products |
|---|---|
| Vitamin D2 Analog | 30 |
| Vitamin D Analog | 27 |
| Vitamin D3 Analog | 9 |
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.