NDC 76420-393 - Diclofenac Sodium

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: 76420-393
Package NDCs from labels: 76420-393-60, 76420-393-14, 76420-393-30, 76420-393-90, 76420-393-01
Manufacturer: ASCLEMED USA INC.
Effective date: 2025-09-24
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Diclofenac Sodium Delayed-release Tablets, USP 75 mg	ASCLEMED USA INC.	2025-09-24	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
76420-393-01	Diclofenac Sodium	100 in 1 BOTTLE	TABLET, DELAYED RELEASE	100	2
76420-393-14	Diclofenac Sodium	14 in 1 BOTTLE	TABLET, DELAYED RELEASE	14	2
76420-393-30	Diclofenac Sodium	30 in 1 BOTTLE	TABLET, DELAYED RELEASE	30	2
76420-393-60	Diclofenac Sodium	60 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	60	2
76420-393-90	Diclofenac Sodium	90 in 1 BOTTLE	TABLET, DELAYED RELEASE	90	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 120 of 124 · 2,480 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diclofenac Sodium Delayed Release	DICLOFENAC SODIUM	Proficient Rx LP	947c0c1f-3573-4f69-ab82-8b50c43e5586	2022-04-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855906 unii: QTG126297Q
Arthritis Pain Reliever	DICLOFENAC SODIUM	CVS PHARMACY, INC	047985ea-f768-4f9a-bfe3-0acf40a4781d	2022-02-15	Warnings	Exact identifier unii: QTG126297Q
basic care arthritis pain	DICLOFENAC SODIUM	Amazon.com Services LLC	a8aa9016-bf2d-4727-9184-512b2570000b	2022-01-06	Warnings	Exact identifier unii: QTG126297Q
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Reported adverse events (FAERS/openFDA)#

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