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
71335-9665_744e72d3-6d43-47d1-9dff-47f4b833e6f8
Product NDC
71335-9665
Form
TABLET, FILM COATED
Composition / generic term
diclofenac sodium
Labeler
Bryant Ranch Prepack
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 (71335-9665-0) · 71335-9665-0
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-1) · 71335-9665-1
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-2) · 71335-9665-2
  • 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-3) · 71335-9665-3
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-4) · 71335-9665-4
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-5) · 71335-9665-5
  • 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-6) · 71335-9665-6
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-7) · 71335-9665-7
  • 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-8) · 71335-9665-8
  • 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-9665-9) · 71335-9665-9

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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