Plumbum mellitum 14

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	48951-8320	48951-8320-1	I	Inactivated by FDA		2026-10-12

Adverse event summaries are temporarily unavailable. Other product information remains available.

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8320-1	Plumbum mellitum 14	10 in 1 BOX	LIQUID	10		2
48951-8320-1	Plumbum mellitum 14	1 mL in 1 AMPULE	LIQUID	1		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8320	PLUMBUM MELLITUM 14 LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 2 package rows	20241027_6bb2b659-2326-5828-e053-2991aa0ab792.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
Y9H1V576FH	HONEY	8028-66-8	HONEY
2P299V784P	LEAD	7439-92-1	LEAD

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-8320-1	48951832001	10 AMPULE in 1 BOX (48951-8320-1) > 1 mL in 1 AMPULE	10 ampule	2009-09-01	0000-00-00	No	No	Current