NDC 82922-017 - 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: 82922-017
Package NDCs from labels: 82922-017-04
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
DIGOXIN - 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 3 of 3 · 44 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Digoxin	DIGOXIN	A-S Medication Solutions	aea39b37-951e-49e8-9756-c763c0e7c7cd	2023-11-24	Warnings, Adverse reactions	Exact identifier unii: 73K4184T59
Digoxin	DIGOXIN	A-S Medication Solutions	0a88434e-4a1b-4ade-a51e-38145e22a232	2023-08-14	Warnings, Adverse reactions	Exact identifier unii: 73K4184T59
ed8b64f7-6d8c-643f-e053-2995a90a0676			e5d78b92-c739-8b66-e053-2995a90a4d8a	2022-11-15		Exact identifier spl set id: e5d78b92-c739-8b66-e053-2995a90a4d8a
LANOXIN	DIGOXIN	Aphena Pharma Solutions - Tennessee, LLC	f6c7ca21-1c76-4838-8fb9-e1bec6001d8b	2019-05-08	Warnings, Adverse reactions	Exact identifier unii: 73K4184T59

Reported adverse events (FAERS/openFDA)#

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