United States · FDA National Drug Code directory
Diclofenac Sodium Delayed Release
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
- 71335-0481_05956d93-ac1e-47fd-b7c8-0817ca13dc70
- Product NDC
- 71335-0481
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Diclofenac Sodium
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19981113
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC SODIUM — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-1) · 71335-0481-1
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-2) · 71335-0481-2
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-3) · 71335-0481-3
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-4) · 71335-0481-4
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-5) · 71335-0481-5
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-6) · 71335-0481-6
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-7) · 71335-0481-7
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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