NDC 82922-014 - 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: 82922-014
Package NDCs from labels: 82922-014-02
Manufacturer: Truemed Group LLC
Effective date: 2022-08-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
FOSAPREPITANT DIMEGLUMINE - Truemed Group LLC	Truemed Group LLC	2022-08-09	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 · 27 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fosaprepitant	FOSAPREPITANT	BluePoint Laboratories	46edae30-d50c-4112-9941-954b13ed5eda	2024-01-18	Warnings, Adverse reactions	Exact identifier unii: D35FM8T64X
Fosaprepitant	FOSAPREPITANT DIMEGLUMINE	NorthStar RxLLC	df341f63-0fef-4411-a89b-6df6b9e792be	2023-07-25	Warnings, Adverse reactions	Exact identifier unii: D35FM8T64X
ed8b0080-09e9-22e4-e053-2a95a90a9096			e5d5f33e-bf59-c442-e053-2995a90a920a	2022-11-15		Exact identifier spl set id: e5d5f33e-bf59-c442-e053-2995a90a920a
Fosaprepitant	FOSAPREPITANT	Novadoz Pharmaceuticals LLC	1e6b36b2-3c8b-4ac4-827e-d6f00d999032	2022-09-30	Warnings, Adverse reactions	Exact identifier unii: D35FM8T64X
Fosaprepitant	FOSAPREPITANT	Actavis Pharma, Inc.	9dbd4c29-d894-4839-9b22-a2f65c8c8ad1	2022-06-30	Warnings, Adverse reactions	Exact identifier unii: D35FM8T64X
Fosaprepitant	FOSAPREPITANT	Novadoz Pharmaceuticals LLC	a7343abe-b2b0-4e5a-907b-532a8e16dfcb	2021-01-01	Warnings, Adverse reactions	Exact identifier unii: D35FM8T64X
Fosaprepitant	FOSAPREPITANT	Dr. Reddy's Laboratories Inc.,	d624667d-ee3b-3501-53fe-da453352042d	2020-03-20	Warnings, Adverse reactions	Exact identifier unii: D35FM8T64X

Reported adverse events (FAERS/openFDA)#

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