NDC 82922-043 - 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: 82922-043
Package NDCs from labels: 82922-043-02
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
PRILOCAINE HYDROCHLORIDE - 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
Citanest Forte DENTAL	PRILOCAINE HCL AND EPINEPHRINE	Novocol Pharmaceutical of Canada, Inc.	801a4f80-397b-46c5-ad3e-a80594e7bda2	2024-02-29	Warnings, Adverse reactions	Exact identifier unii: MJW015BAPH
Citanest Forte DENTAL	PRILOCAINE HCL AND EPINEPHRINE	Dentsply Pharmaceutical Inc.	60c8710b-ae55-4fdf-e053-2991aa0adc75	2024-02-29	Warnings, Adverse reactions	Exact identifier unii: MJW015BAPH
ed8b5178-6f86-4cc6-e053-2995a90a8a3d			e5fd773f-7b07-da83-e053-2a95a90a654c	2022-11-15		Exact identifier spl set id: e5fd773f-7b07-da83-e053-2a95a90a654c
Citanest Plain	PRILOCAINE HYDROCHLORIDE	Dentsply Pharmaceutical Inc.	db23a56f-1e41-4843-9220-1b2e3059db41	2021-11-10	Warnings, Adverse reactions	Exact identifier unii: MJW015BAPH

Reported adverse events (FAERS/openFDA)#

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