FDA.reportPublic FDA data

Ludens Kiwi-Strawberry

Product NDC
52183-205
11-digit product format
521830205
Labeler code
52183
Product ID
52183-205_db3a062d-41f4-40b1-8706-aa1d9694e61d
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
2012-07-02
Marketing end
2021-05-31
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.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct52183-205DDiscontinued by firm2026-07-31
excluded packagepackage52183-20552183-205-20DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52183-205-205218302052020 LOZENGE in 1 BAG (52183-205-20) 20 lozenge2012-07-022021-05-31NoNoCurrent