FDA NDC Directory · JSON-LD · Markdown
NDC 0173-0873 · HUMAN PRESCRIPTION DRUG · AEROSOL, POWDER
| Generic name | umeclidinium |
|---|---|
| Labeler / Manufacturer | GlaxoSmithKline LLC |
| Marketing category | New Drug Application (innovator) · App NDA205382 |
| Dosage form / route | AEROSOL, POWDER · ORAL |
| Active ingredients | UMECLIDINIUM BROMIDE (62.5 ug/1) |
| Marketing started | 20140430 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).