United States · FDA National Drug Code directory
Diclofenac Potassium
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
- 69306-750_42fd182d-4a2e-7058-e063-6294a90a63f9
- Product NDC
- 69306-750
- Form
- TABLET, FILM COATED
- Composition / generic term
- diclofenac potassium
- Labeler
- Doc Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241021
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC POTASSIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69306-750-03) · 69306-750-03
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 →