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
- 50090-7838_8a5992ce-44cc-460a-970e-4d7b5ac068e5
- Product NDC
- 50090-7838
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Diclofenac Sodium
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250328
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC SODIUM — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-0) · 50090-7838-0
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-1) · 50090-7838-1
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-2) · 50090-7838-2
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-3) · 50090-7838-3
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-4) · 50090-7838-4
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-8) · 50090-7838-8
- 180 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7838-9) · 50090-7838-9
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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