NDC product
POWDER · Pharmacia and Upjohn Company LLC
NDC 0009-5164 · Pharmacia and Upjohn Company LLC
Key facts
| Product NDC | 0009-5164 |
|---|---|
| Nonproprietary name | Epoprostenol Sodium |
| Substances | EPOPROSTENOL SODIUM |
| Dosage form | POWDER |
| Labeler | Pharmacia and Upjohn Company LLC |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Jul 3, 2014 |
| 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: