United States · FDA National Drug Code directory

Diclofenac Sodium

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
60429-421_52d448a2-01fb-19f8-e063-6294a90ab893
Product NDC
60429-421
Form
TABLET, DELAYED RELEASE
Composition / generic term
Diclofenac Sodium
Labeler
Golden State Medical Supply, Inc.
Marketing category
ANDA
Marketing start / end (source format)
19960326 / 20270430

Source-listed ingredients

  • DICLOFENAC SODIUM — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (60429-421-01) · 60429-421-01
  • 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (60429-421-10) · 60429-421-10

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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