NDC product
Hydro 35
NDC 23710-035 · Exeltis USA Dermatology, LLC
Key facts
| Product NDC | 23710-035 |
|---|---|
| Proprietary name | Hydro 35 |
| Labeler | Exeltis USA Dermatology, LLC |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jun 20, 2009 |
| Marketing end | Jan 20, 2020 |
| Listing certified through | Jan 20, 2020 |
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: