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
75834-264_542fd9dd-a6d3-4432-9e7a-2ca5bce12956
Product NDC
75834-264
Form
TABLET, DELAYED RELEASE
Composition / generic term
diclofenac sodium and misoprostol
Labeler
Nivagen Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20210715
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 (75834-264-60) · 75834-264-60
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (75834-264-90) · 75834-264-90

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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