NDC product
Antifungal Liquid Maximum Strength
NDC 0363-7998 · Walgreens Company
Key facts
| Product NDC | 0363-7998 |
|---|---|
| Proprietary name | Antifungal Liquid Maximum Strength |
| Nonproprietary name | Tolnaftate |
| Substances | TOLNAFTATE |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Walgreens Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M005 |
| Marketing start | Mar 12, 2024 |
| Marketing end | Nov 30, 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