NDC product
Zeasorb
NDC 0316-0232 · Crown Laboratories
Key facts
| Product NDC | 0316-0232 |
|---|---|
| Proprietary name | Zeasorb |
| Labeler | Crown Laboratories |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M005 |
| Marketing start | Mar 14, 2011 |
| Marketing end | Apr 16, 2025 |
| Listing certified through | Apr 16, 2025 |
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: