NDC product
SYMBICORT
NDC 0186-0370 · AstraZeneca Pharmaceuticals LP
Key facts
| Product NDC | 0186-0370 |
|---|---|
| Proprietary name | SYMBICORT |
| Nonproprietary name | Budesonide and Formoterol Fumarate Dihydrate |
| Substances | BUDESONIDE, FORMOTEROL FUMARATE |
| Dosage form | AEROSOL |
| Route | RESPIRATORY (INHALATION) |
| Labeler | AstraZeneca Pharmaceuticals LP |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA021929 |
| Pharmacologic classes | Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC] |
| Marketing start | May 29, 2007 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: