NDC 82922-042 - 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: 82922-042
Package NDCs from labels: 82922-042-07
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
HETASTARCH - 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 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hextend	HETASTARCH	Hospira, Inc.	fc79700c-6c3b-4998-8307-4dc8c81c5041	2026-05-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 875Y4127EA
Hetastarch in Sodium Chloride	HETASTARCH	Hospira, Inc.	d64f961a-3e1f-4b04-cf83-604474af2775	2026-04-30	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 875Y4127EA
6% HETASTARCH IN 0.9% SODIUM CHLORIDE	6% HETASTARCH IN 0.9% SODIUM CHLORIDE	HF Acquisition Co LLC, DBA HealthFirst	7b97c681-4514-c544-e053-2991aa0a3d78	2024-01-29	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 875Y4127EA
ed8b3c3c-fd15-a1aa-e053-2995a90ab160			e5fd551f-048c-f431-e053-2a95a90adacd	2022-11-15		Exact identifier spl set id: e5fd551f-048c-f431-e053-2a95a90adacd

Reported adverse events (FAERS/openFDA)#

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