Ludens
- Product NDC
- 52183-210
- 11-digit product format
- 521830210
- Labeler code
- 52183
- Product ID
- 52183-210_fa852297-5b7c-4e87-9bc5-a91cea72116f
- 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
- 2017-04-01
- Marketing end
- 2020-07-31
- Substance
- PECTIN
- Active strength
- 3 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 52183-210 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 52183-210 | 52183-210-25 | D | Discontinued by firm | 2026-07-31 |