NDC product
Ludens Wild Cherry Throat Drops
NDC 52183-229 · Prestige Brands Holdings, Inc.
Key facts
| Product NDC | 52183-229 |
|---|---|
| Proprietary name | Ludens Wild Cherry Throat Drops |
| Nonproprietary name | Pectin |
| Substances | PECTIN |
| 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 | Oct 29, 2009 |
| Listing certified through | Dec 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 · Source date: