United States · FDA National Drug Code directory
Diclofenac Sodium
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
- 43063-467_4d52a1c6-bbc0-0b02-e063-6294a90afa45
- Product NDC
- 43063-467
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Diclofenac Sodium
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19960326
- Source listing expiry
- 20271231
Source-listed ingredients
- DICLOFENAC SODIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-14) · 43063-467-14
- 15 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-15) · 43063-467-15
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-20) · 43063-467-20
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-467-30) · 43063-467-30
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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