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
- 68001-232_3e847cfc-d342-3a15-e063-6394a90aeb46
- Product NDC
- 68001-232
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Diclofenac Sodium and Misoprostol
- Labeler
- BluePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140226
- 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 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-232-06) · 68001-232-06
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 →