Data / Drug companies / Budesonide and formoterol fumarate dihydrate
Budesonide and formoterol fumarate dihydrate: 5 companies and 15 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Budesonide and formoterol fumarate dihydrate is listed in the FDA National Drug Code Directory by 5 companies, with 15 products in commercial distribution. 2 of the products (13.3%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are aerosol; aerosol, metered, and the newest product started marketing on May 27, 2026.
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- Companies listing it
- 5
- Products
- 15
- Generic (ANDA) products
- 2 (13.3%)
- Application numbers
- 2
- Routes
- Respiratory (inhalation)
- Brand names
- Symbicort
- openFDA record search
- api.fda.gov
Companies that list budesonide and formoterol fumarate dihydrate
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 6 | aerosol | New drug applications (NDA) | January 3, 2020 |
| Sportpharm LLC | 3 | aerosol | Authorized generics (NDA) | January 3, 2020 |
| AstraZeneca Pharmaceuticals LP | 2 | aerosol | New drug applications (NDA) | May 29, 2007 |
| AstraZeneca Pharmaceuticals LP | 2 | aerosol | Authorized generics (NDA) | January 3, 2020 |
| Teva Pharmaceuticals, Inc. | 2 | aerosol, metered | Generic drugs (ANDA) | May 27, 2026 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Aerosol | 13 | 86.7% |
| Aerosol, metered | 2 | 13.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 7 | 46.7% |
| Authorized generics (NDA) | 6 | 40% |
| Generic drugs (ANDA) | 2 | 13.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Corticosteroid | 15 |
| beta2-Adrenergic Agonist | 15 |
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.