NDC 70518-4564-00 - Guanfacine

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: 70518-4564
Requested NDC: 70518-4564-00
Package NDCs from labels: 70518-4564-0, 70518-4564-00
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-02-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Guanfacine Tablets, USP Rx only	REMEDYREPACK INC.	2026-02-03	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-4564-0	Guanfacine	30 in 1 BLISTER PACK	TABLET	30		1

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 4 of 4 · 62 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Guanfacine	GUANFACINE	Proficient Rx LP	09442806-db7b-49de-8ffc-e4cb83138349	2020-07-01	Adverse reactions	Exact identifier rxcui: 197745 unii: PML56A160O
guanfacine	GUANFACINE	Actavis Pharma, Inc.	3a171942-37af-430d-8b9d-bb678ca2be4b	2020-01-31	Warnings, Adverse reactions	Exact identifier unii: PML56A160O

Reported adverse events (FAERS/openFDA)#

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