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
85766-032_4a2b79c2-3d4a-4fe7-e063-6394a90a3acb
Product NDC
85766-032
Form
TABLET, FILM COATED
Composition / generic term
diclofenac sodium
Labeler
Sportpharm LLC
Marketing category
ANDA
Marketing start / end (source format)
20220926
Source listing expiry
20271231

Source-listed ingredients

  • DICLOFENAC SODIUM — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-01) · 85766-032-01
  • 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-07) · 85766-032-07
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-14) · 85766-032-14
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-20) · 85766-032-20
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-30) · 85766-032-30
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-60) · 85766-032-60
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85766-032-90) · 85766-032-90

Source and coverage

Open FDA National Drug Code directory

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 — United States | Molindra Medicines