United States · FDA National Drug Code directory

Diclofenac Sodium Delayed Release

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 63629-2013_ae287719-9402-4581-86ca-b017a1ad99c3
Product NDC: 63629-2013
Form: TABLET, DELAYED RELEASE
Composition / generic term: Diclofenac Sodium
Labeler: Bryant Ranch Prepack
Marketing category: ANDA
Marketing start / end (source format): 19981113
Source listing expiry: 20261231

Source-listed ingredients

DICLOFENAC SODIUM — 75 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

24 BOTTLE, PLASTIC in 1 BOX (63629-2013-1) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 63629-2013-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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