ACONITE NAPELLIS

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	54973-0600		D	Discontinued by firm		2026-08-03
excluded package	package	54973-0600	54973-0600-4	D	Discontinued by firm		2026-08-03

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACONITUM NAPELLUS ROOT	ACTIVE INGREDIENT	KPD2N7348X	ACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]	1
ACONITUM NAPELLUS ROOT	ACTIVE MOIETY	KPD2N7348X	ACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]	1
ACACIA	INACTIVE INGREDIENT	5C5403N26O	ACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	ACONITE NAPELLIS (ACONITUM NAPELLUS ROOT) TABLET [HYLAND'S]	1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
KPD2N7348X	ACONITUM NAPELLUS ROOT	8063-12-5	ACONITUM NAPELLUS ROOT

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
54973-0600-4	54973060004	250 TABLET in 1 BOTTLE, PLASTIC (54973-0600-4)	250 tablet	1955-01-01	0000-00-00	No	No	Current