NDC 82922-018 - 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: 82922-018
Package NDCs from labels: 82922-018-02
Manufacturer: Truemed Group LLC
Effective date: 2022-08-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
DIAZOXIDE - Truemed Group LLC	Truemed Group LLC	2022-08-10	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 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diazoxide	DIAZOXIDE	Par Health USA, LLC	abe317a5-6c63-469c-89c8-9fedfe859c3d	2026-08-07	Warnings, Adverse reactions	Exact identifier unii: O5CB12L4FN
Diazoxide	DIAZOXIDE	e5 Pharma, LLC	c0237320-2d3f-4907-a4d3-08f138aa4ca8	2025-07-31	Warnings, Adverse reactions	Exact identifier unii: O5CB12L4FN
ed8b6a2d-20bc-6ef0-e053-2995a90a1ead			e5e5624d-3a61-0f30-e053-2a95a90a7609	2022-11-15		Exact identifier spl set id: e5e5624d-3a61-0f30-e053-2a95a90a7609

Reported adverse events (FAERS/openFDA)#

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