NDC product
Prochlorperazine Edisylate
NDC 0641-6225 · Hikma Pharmaceuticals USA Inc.
Key facts
| Product NDC | 0641-6225 |
|---|---|
| Proprietary name | Prochlorperazine Edisylate |
| Labeler | Hikma Pharmaceuticals USA Inc. |
| Marketing category | ANDA |
| Application number | ANDA213630 |
| Marketing start | Jan 2, 2023 |
| Marketing end | Jul 29, 2024 |
| Listing certified through | Jul 29, 2024 |
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: