Ludens Assorted Flavors
- Product NDC
- 52183-217
- 11-digit product format
- 521830217
- Labeler code
- 52183
- Product ID
- 52183-217_973b7e0f-910d-440d-aadc-3e4f5b795c11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pectin
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Prestige Brands Holdings, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-06-13
- Marketing end
- 0000-00-00
- Substance
- PECTIN
- Active strength
- 3 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 52183-217 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 52183-217 | 52183-217-90 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 52183-217-90 | 52183021790 | 90 LOZENGE in 1 BAG (52183-217-90) | 90 lozenge | 2017-06-13 | 0000-00-00 | No | No | Current |