Rheuma

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	48951-8350		I	Inactivated by FDA		2026-10-12
excluded package	package	48951-8350	48951-8350-5	I	Inactivated by FDA		2026-10-12

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

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8350-5	Rheuma	60 g in 1 TUBE	OINTMENT	60		3

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8350	RHEUMA OINTMENT [URIEL PHARMACY INC.]	3	Legacy NDC, 1 package rows	20241206_77f9073d-62d7-7d71-e053-2991aa0a51c9.zip

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-8350-5	48951835005	60 g in 1 TUBE (48951-8350-5)	60 g	2009-09-01	0000-00-00	No	No	Current