NDC product
Curosurf
NDC 10122-510 · Chiesi USA, Inc.
Key facts
| Product NDC | 10122-510 |
|---|---|
| Proprietary name | Curosurf |
| Nonproprietary name | poractant alfa |
| Substances | PORACTANT ALFA |
| Dosage form | SUSPENSION |
| Route | ENDOTRACHEAL |
| Labeler | Chiesi USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Application number | BLA020744 |
| Pharmacologic classes | Alveolar Surface Tension Reduction [PE], Surfactant Activity [MoA], Surfactant [EPC] |
| Marketing start | Nov 18, 1999 |
| 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: