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
51655-280_48e702c3-71aa-a566-e063-6394a90a7778
Product NDC
51655-280
Form
TABLET, DELAYED RELEASE
Composition / generic term
Diclofenac Sodium
Labeler
Northwind Health Company, LLC
Marketing category
ANDA
Marketing start / end (source format)
20221026
Source listing expiry
20271231

Source-listed ingredients

  • DICLOFENAC SODIUM — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-26) · 51655-280-26
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-280-52) · 51655-280-52

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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Diclofenac Sodium Delayed Release — United States | Molindra Medicines