Ludens Assorted Flavors
- Product NDC
- 52183-217
- Requested package NDC
- 52183-217-90
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52183-217 | LUDENS ASSORTED FLAVORS (PECTIN) LOZENGE [PRESTIGE BRANDS HOLDINGS, INC.] | 3 | Legacy NDC | 20241116_60d6da81-e128-4a9b-88de-39c48511196f.zip |
Packages#
Package NDC, 11-digit format, Description table| 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 |