Cuprum 12

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	48951-3238		I	Inactivated by FDA		2026-08-17
excluded package	package	48951-3238	48951-3238-3	I	Inactivated by FDA		2026-08-17

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-3238-3	Cuprum 12	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-3238	CUPRUM 12 LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20201216_b684a828-3264-87f6-e053-2a95a90a984b.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
789U1901C5	COPPER	7440-50-8	COPPER

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-3238-3	48951323803	60 mL in 1 BOTTLE, DROPPER (48951-3238-3)	60 ml	2009-09-01	0000-00-00	No	No	Current