United States · FDA National Drug Code directory
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
- 71335-2455_b36894f2-8cb1-41ac-87b1-dae08dd0f517
- Product NDC
- 71335-2455
- Form
- TABLET
- Composition / generic term
- Misoprostol
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220411
- Source listing expiry
- 20271231
Source-listed ingredients
- MISOPROSTOL — 100 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET in 1 BOTTLE (71335-2455-1) · 71335-2455-1
- 90 TABLET in 1 BOTTLE (71335-2455-2) · 71335-2455-2
- 30 TABLET in 1 BOTTLE (71335-2455-3) · 71335-2455-3
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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