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
75834-337_4580c689-1082-1dc8-e063-6294a90afff4
Product NDC
75834-337
Form
TABLET, FILM COATED
Composition / generic term
Diclofenac Potassium Tablets
Labeler
NIVAGEN PHARMACEUTICALS, INC.
Marketing category
ANDA
Marketing start / end (source format)
20251010
Source listing expiry
20261231

Source-listed ingredients

  • DICLOFENAC POTASSIUM — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (75834-337-30) · 75834-337-30
  • 60 TABLET, FILM COATED in 1 BOTTLE (75834-337-60) · 75834-337-60

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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