United States · FDA National Drug Code directory
Diclofenac Sodium/Misoprostol 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
- 42571-134_3afc5367-562f-b4a0-e063-6294a90a2560
- Product NDC
- 42571-134
- Form
- TABLET
- Composition / generic term
- Diclofenac Sodium/Misoprostol
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- 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
- 60 BLISTER PACK in 1 CARTON (42571-134-29) / 10 TABLET in 1 BLISTER PACK · 42571-134-29
- 30 TABLET in 1 BOTTLE (42571-134-30) · 42571-134-30
- 60 TABLET in 1 BOTTLE (42571-134-60) · 42571-134-60
- 90 TABLET in 1 BOTTLE (42571-134-90) · 42571-134-90
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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