NDC product
Antifungal Pen
NDC 85210-001 · XF Agencija Limited
Key facts
| Product NDC | 85210-001 |
|---|---|
| Proprietary name | Antifungal Pen |
| Nonproprietary name | UNDECYLENIC ACID 25% |
| Substances | UNDECYLENIC ACID |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | XF Agencija Limited |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M005 |
| Marketing start | Jan 28, 2025 |
| Listing certified through | Dec 31, 2026 |
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: