United States · FDA National Drug Code directory
Diclofenac Sodium and Misoprostol
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
- 71335-1183_3c1e7d73-b9c0-4260-87ed-049797c1e8dc
- Product NDC
- 71335-1183
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Diclofenac Sodium and Misoprostol
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161201
- Source listing expiry
- 20261231
Source-listed ingredients
- DICLOFENAC SODIUM — 75 mg/1
- MISOPROSTOL — 200 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-1) · 71335-1183-1
- 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-2) · 71335-1183-2
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-3) · 71335-1183-3
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-4) · 71335-1183-4
- 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-5) · 71335-1183-5
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 →