Argentum 21X

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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	48951-1328		I	Inactivated by FDA		2026-08-11
excluded package	package	48951-1328	48951-1328-1	I	Inactivated by FDA		2026-08-11

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-1328-1	2026-01-29	C162847	48780-1	49896155-ac06-586f-e063-e6dba90add90	Argentum 21X

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1328-1	Argentum 21X	1 mL in 1 AMPULE	LIQUID	1		2
48951-1328-1	Argentum 21X	10 in 1 BOX	LIQUID	10		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1328	ARGENTUM 21X LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 2 package rows	20240402_969c0200-c8a5-0517-e053-2a95a90aa264.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3M4G523W1G	SILVER	7440-22-4	SILVER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1328-1	48951132801	10 AMPULE in 1 BOX (48951-1328-1) > 1 mL in 1 AMPULE	10 ampule	2019-11-05	0000-00-00	No	No	Current