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
- 51672-1363_38ef9dc7-662f-056c-e063-6394a90a47e2
- Product NDC
- 51672-1363
- Form
- GEL
- Composition / generic term
- diclofenac sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160428
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC SODIUM — 30 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-1363-3) / 50 g in 1 TUBE · 51672-1363-3
- 1 TUBE in 1 CARTON (51672-1363-7) / 100 g in 1 TUBE · 51672-1363-7
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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