NDC 82922-047 - Truemed Group LLC

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 82922-047
Package NDCs from labels: 82922-047-01
Manufacturer: Truemed Group LLC
Effective date: 2022-08-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
LEFLUNOMIDE - Truemed Group LLC	Truemed Group LLC	2022-08-11	HUMAN PRESCRIPTION DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 2 · 26 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
leflunomide	LEFLUNOMIDE	Bryant Ranch Prepack	af4079af-c127-476e-a2b3-53b438dc9da4	2024-08-12	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: G162GK9U4W
leflunomide	LEFLUNOMIDE	Zydus Pharmaceuticals (USA) Inc.	b9af9870-014f-4c4e-8738-bb04b30b3e85	2024-08-12	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: G162GK9U4W
leflunomide	LEFLUNOMIDE	Zydus Lifesciences Limited	c66cacd1-93f7-483a-a2fc-aad53d5342b0	2024-08-12	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: G162GK9U4W
Leflunomide	LEFLUNOMIDE	Aurobindo Pharma Limited	c358276a-610e-46da-b81a-95c837af205d	2024-08-07	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: G162GK9U4W
Leflunomide	LEFLUNOMIDE	Alembic Pharmaceuticals Limited	f6a4107e-b393-45ed-8e5a-70af5bd53826	2023-01-30	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: G162GK9U4W
ed8b1625-9aac-7720-e053-2995a90a648b			e5fdd055-4f64-1172-e053-2a95a90a678f	2022-11-15		Exact identifier spl set id: e5fdd055-4f64-1172-e053-2a95a90a678f

Reported adverse events (FAERS/openFDA)#

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