FDA NDC Directory · JSON-LD · Markdown
NDC 0186-0372 · HUMAN PRESCRIPTION DRUG · AEROSOL
| Generic name | Budesonide and Formoterol Fumarate Dihydrate |
|---|---|
| Labeler / Manufacturer | AstraZeneca Pharmaceuticals LP |
| Marketing category | New Drug Application (innovator) · App NDA021929 |
| Dosage form / route | AEROSOL · RESPIRATORY (INHALATION) |
| Active ingredients | BUDESONIDE (80 ug/1) FORMOTEROL FUMARATE (4.5 ug/1) |
| Marketing started | 20070529 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).