Data / Drug companies / Opella Healthcare International Sas
Opella Healthcare International Sas: 17 products in the FDA NDC directory, labeler code 12579
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Opella Healthcare International Sas (labeler code 12579) lists 17 products in the FDA National Drug Code Directory. By type: 15 drugs for further processing, 2 bulk ingredients. Its main marketing category is drugs for further processing. The newest product started marketing on April 3, 2026.
The request: Watch Opella Healthcare International Sas (FDA labeler code 12579): each new product listing and each discontinued product. $10 of work on sign-up, no card.
SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.
- Labeler code
- 12579
- Products in commercial distribution
- 17
- Packages
- 19
- Finished drugs by generic name
- 0
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 1
- Earliest marketing start
- September 10, 1998
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Drugs for further processing | 15 | 88.2% |
| Bulk ingredients for compounding | 2 | 11.8% |
Products by type
| Type | Products | Share |
|---|---|---|
| Drugs for further processing | 15 | 88.2% |
| Bulk ingredients | 2 | 11.8% |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 6 | 35.3% |
| Tablet | 4 | 23.5% |
| Tablet, film coated, extended release | 3 | 17.6% |
| Tablet, coated | 3 | 17.6% |
| Tablet, orally disintegrating | 1 | 5.9% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Fexofenadine hydrochloride | 12579-181 | Tablet, film coated, extended release | Drugs for further processing | April 3, 2026 |
| Tadalafil | 12579-200 | Tablet, coated | Drugs for further processing | July 1, 2025 |
| Levocetirizine dihydrochloride | 12579-180 | Tablet | Drugs for further processing | March 22, 2024 |
| Bisacodyl | 12579-230 | Tablet, coated | Drugs for further processing | September 3, 2019 |
| Bisacodyl | 12579-228 | Tablet, coated | Drugs for further processing | September 3, 2019 |
| Fexofenadine hydrochloride | 12579-189 | Tablet, film coated, extended release | Drugs for further processing | April 16, 2014 |
| Teriflunomide | 12579-191 | Tablet, film coated | Drugs for further processing | May 1, 2013 |
| Teriflunomide | 12579-190 | Tablet, film coated | Drugs for further processing | May 1, 2013 |
| Teriflunomide | 12579-186 | Tablet, film coated | Drugs for further processing | September 13, 2012 |
| Teriflunomide | 12579-185 | Tablet, film coated | Drugs for further processing | September 13, 2012 |
| Fexofenadine hydrochloride | 12579-182 | Tablet, film coated, extended release | Drugs for further processing | March 1, 2012 |
| Glyburide | 12579-056 | Tablet | Drugs for further processing | November 16, 2011 |
| Glyburide | 12579-055 | Tablet | Drugs for further processing | November 16, 2011 |
| Glyburide | 12579-054 | Tablet | Drugs for further processing | November 16, 2011 |
| Fexofenadine hydrochloride | 12579-188 | Tablet, orally disintegrating | Drugs for further processing | March 3, 2011 |
| Leflunomide | 12579-510 | Tablet, film coated | Bulk ingredients for compounding | September 10, 1998 |
| Leflunomide | 12579-509 | Tablet, film coated | Bulk ingredients for compounding | September 10, 1998 |
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.