NDC product
Siltussin SA
NDC 17856-0117 · Atlantic Biologicals Corps
Key facts
| Product NDC | 17856-0117 |
|---|---|
| Proprietary name | Siltussin SA |
| Labeler | Atlantic Biologicals Corps |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Oct 5, 1998 |
| Marketing end | Oct 16, 2019 |
| Listing certified through | Oct 16, 2019 |
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: