NDC product
Sunmark
NDC 17856-0832 · ATLANTIC BIOLOGICALS CORP.
Key facts
| Product NDC | 17856-0832 |
|---|---|
| Proprietary name | Sunmark |
| Labeler | ATLANTIC BIOLOGICALS CORP. |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M |
| Marketing start | Apr 10, 2019 |
| Marketing end | Jul 18, 2025 |
| Listing certified through | Jul 18, 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: