NDC product
Divalproex Sodium Delayed Release (Sprinkle)
NDC 0781-2243 · Sandoz Inc.
Key facts
| Product NDC | 0781-2243 |
|---|---|
| Proprietary name | Divalproex Sodium |
| Labeler | Sandoz Inc. |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA019680 |
| Marketing start | Aug 31, 2015 |
| Marketing end | Nov 5, 2021 |
| Listing certified through | Nov 5, 2021 |
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: