FDA.reportPublic FDA data

Ludens

Product NDC
52183-212
Requested package NDC
52183-212-25
11-digit product format
521830212
Labeler code
52183
Product ID
52183-212_220c0e48-cfca-4a78-83da-5b75432ceed6
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
2017-07-01
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#

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.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage52183-21252183-212-25DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52183-212-255218302122525 LOZENGE in 1 BAG (52183-212-25) 25 lozenge2017-07-010000-00-00NoNoCurrent