NDC product
Ludens Dual Relief
NDC 52183-227 · Prestige Brands Holdings, Inc.
Key facts
| Product NDC | 52183-227 |
|---|---|
| Proprietary name | Ludens |
| Nonproprietary name | pectin and menthol |
| Substances | PECTIN, MENTHOL |
| Dosage form | LOZENGE |
| Route | ORAL |
| Labeler | Prestige Brands Holdings, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M022 |
| Marketing start | Jun 15, 2018 |
| Marketing end | Mar 31, 2027 |
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