NDC 70518-4364-01 - CHLORZOXAZONE

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: 70518-4364
Requested NDC: 70518-4364-01
Package NDCs from labels: 70518-4364-0, 70518-4364-1, 70518-4364-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-01-29
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Chlorzoxazone Tablets, USP	REMEDYREPACK INC.	2026-01-29	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-4364-0	CHLORZOXAZONE	90 in 1 BOTTLE, PLASTIC	TABLET	90		2
70518-4364-1	CHLORZOXAZONE	60 in 1 BOTTLE, PLASTIC	TABLET	60		2

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 · 41 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Chlorzoxazone	CHLORZOXAZONE	Novitium Pharma LLC	69c87a85-4b6b-405b-9fa5-4c91c0f90c70	2021-10-29	Warnings, Adverse reactions	Exact identifier rxcui: 197502 unii: H0DE420U8G

Reported adverse events (FAERS/openFDA)#

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