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
- 63629-4108_37d9b7c1-4bf8-44ed-8d48-bd1ee6efd72c
- Product NDC
- 63629-4108
- Form
- TABLET, FILM COATED
- Composition / generic term
- Diclofenac Potassium
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19980811
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC POTASSIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (63629-4108-1) · 63629-4108-1
- 90 TABLET, FILM COATED in 1 BOTTLE (63629-4108-2) · 63629-4108-2
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-4108-3) · 63629-4108-3
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-4108-4) · 63629-4108-4
- 45 TABLET, FILM COATED in 1 BOTTLE (63629-4108-5) · 63629-4108-5
- 58 TABLET, FILM COATED in 1 BOTTLE (63629-4108-6) · 63629-4108-6
- 18 TABLET, FILM COATED in 1 BOTTLE (63629-4108-7) · 63629-4108-7
- 120 TABLET, FILM COATED in 1 BOTTLE (63629-4108-8) · 63629-4108-8
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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