United States · FDA National Drug Code directory
Diclofenac Sodium 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
- 71205-866_47a851b9-3e7f-4271-a2b8-ce836579729b
- Product NDC
- 71205-866
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Diclofenac Sodium and Misoprostol
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210715
- 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
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-00) · 71205-866-00
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-30) · 71205-866-30
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-55) · 71205-866-55
- 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-60) · 71205-866-60
- 240 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-64) · 71205-866-64
- 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-72) · 71205-866-72
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-866-90) · 71205-866-90
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 →