Aconitum e tub. 6 Special Order

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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	48951-1236	48951-1236-1	D	Discontinued by firm		2026-07-31

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACONITUM NAPELLUS	ACTIVE INGREDIENT	U0NQ8555JD	ACONITUM E TUB. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
ACONITUM NAPELLUS	ACTIVE MOIETY	U0NQ8555JD	ACONITUM E TUB. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	ACONITUM E TUB. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ACONITUM E TUB. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
U0NQ8555JD	ACONITUM NAPELLUS	ACONITUM NAPELLUS

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1236-1	48951123601	10 AMPULE in 1 BOX (48951-1236-1) > 1 mL in 1 AMPULE	10 ampule	2009-09-01	0000-00-00	No	No	Current