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
42291-232_4dc7edc1-b426-ac49-e063-6294a90af71b
Product NDC
42291-232
Form
TABLET, DELAYED RELEASE
Composition / generic term
Diclofenac Sodium and Misoprostol
Labeler
AvKARE
Marketing category
ANDA
Marketing start / end (source format)
20121214
Source listing expiry
20271231

Source-listed ingredients

  • DICLOFENAC SODIUM — 50 mg/1
  • MISOPROSTOL — 200 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-232-60) · 42291-232-60

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 →