Ludens

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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	52183-225		D	Discontinued by firm		2026-07-31
excluded package	package	52183-225	52183-225-25	D	Discontinued by firm		2026-07-31

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52183-225-25	2020-07-01	C162847	48780-1	9d75b9d0-9013-f424-e053-dadaa90a57ce	Ludens Dual Relief Wild Cherry - 52183-225-25
52183-225-25	2020-01-31	C162847	48780-1	9d75b9d0-9013-f424-e053-dadaa90a57ce	Ludens Dual Relief Wild Cherry - 52183-225-25

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
89NA02M4RX	PECTIN	9000-69-5	PECTIN

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52183-225-25	52183022525	25 LOZENGE in 1 BAG (52183-225-25)	25 lozenge	2018-06-15	2023-09-30	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Ludens Dual Relief Wild Cherry - 52183-225-25	Prestige Brands Holdings, Inc.	2020-07-02	HUMAN OTC DRUG LABEL	2