Ludens
- Product NDC
- 52183-225
- 11-digit product format
- 521830225
- Labeler code
- 52183
- Product ID
- 52183-225_e27dac46-31e8-4925-940c-1eef27b16771
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pectin and menthol
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Prestige Brands Holdings, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-06-15
- Marketing end
- 2023-09-30
- Substance
- PECTIN; MENTHOL
- Active strength
- 3 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52183-225-25 | 52183022525 | 25 LOZENGE in 1 BAG (52183-225-25) | 25 lozenge | 2018-06-15 | 2023-09-30 | No | No | Current |