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
50090-5893_b6546725-2742-4aef-a3cf-0c53aeaea638
Product NDC
50090-5893
Form
TABLET, COATED
Composition / generic term
diclofenac potassium
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20201219
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, COATED in 1 BOTTLE (50090-5893-0) · 50090-5893-0
  • 21 TABLET, COATED in 1 BOTTLE (50090-5893-1) · 50090-5893-1
  • 45 TABLET, COATED in 1 BOTTLE (50090-5893-3) · 50090-5893-3
  • 90 TABLET, COATED in 1 BOTTLE (50090-5893-4) · 50090-5893-4

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.

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Diclofenac Potassium — United States | Molindra Medicines