United States · FDA National Drug Code directory
Arthritis Pain Reliever
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
- 59726-012_4a226f9f-95f7-47bf-8f9e-741ecea07fe1
- Product NDC
- 59726-012
- Form
- GEL
- Composition / generic term
- Diclofenac sodium
- Labeler
- P & L Development, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210625
- 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 (59726-012-50) / 50 g in 1 TUBE · 59726-012-50
- 1 TUBE in 1 CARTON (59726-012-53) / 100 g in 1 TUBE · 59726-012-53
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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