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
- 72162-1734_daaf314b-5e73-4b47-895a-19f37bea7a0b
- Product NDC
- 72162-1734
- 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 — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-0) · 72162-1734-0
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-1) · 72162-1734-1
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-3) · 72162-1734-3
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-4) · 72162-1734-4
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-5) · 72162-1734-5
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-6) · 72162-1734-6
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-7) · 72162-1734-7
- 15 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-8) · 72162-1734-8
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72162-1734-9) · 72162-1734-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →