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
69097-720_930f1c44-2aea-41a8-a9d8-feb8e2699b9f
Product NDC
69097-720
Form
GEL
Composition / generic term
Diclofenac sodium
Labeler
Cipla USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240805
Source listing expiry
20261231

Source-listed ingredients

  • DICLOFENAC SODIUM — 10 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (69097-720-44) / 100 g in 1 TUBE · 69097-720-44

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.

Browse United States records →