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
- 54348-148_ea92d79f-b58c-2ad8-e053-2a95a90acafb
- Product NDC
- 54348-148
- Form
- TABLET
- Composition / generic term
- MISOPROSTOL
- Labeler
- PharmPak, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190710
- Source listing expiry
- 20261231
Source-listed ingredients
- MISOPROSTOL — 200 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 BOX (54348-148-00) / 1 TABLET in 1 BOTTLE · 54348-148-00
- 1 BOTTLE in 1 BOX (54348-148-01) / 1 TABLET in 1 BOTTLE · 54348-148-01
- 1 BOTTLE in 1 BOX (54348-148-02) / 2 TABLET in 1 BOTTLE · 54348-148-02
- 1 BOTTLE in 1 BOX (54348-148-03) / 3 TABLET in 1 BOTTLE · 54348-148-03
- 1 BOTTLE in 1 BOX (54348-148-04) / 4 TABLET in 1 BOTTLE · 54348-148-04
- 1 BOTTLE in 1 BOX (54348-148-06) / 6 TABLET in 1 BOTTLE · 54348-148-06
- 1 BOTTLE in 1 BOX (54348-148-08) / 8 TABLET in 1 BOTTLE · 54348-148-08
- 1 BOTTLE in 1 BOX (54348-148-09) / 9 TABLET in 1 BOTTLE · 54348-148-09
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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