United States · FDA National Drug Code directory
MOVANTIK
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
- 82625-8801_5a6f698f-5b0a-94f1-e063-6394a90a5d4b
- Product NDC
- 82625-8801
- Form
- TABLET, FILM COATED
- Composition / generic term
- naloxegol oxalate
- Labeler
- Averitas Pharma, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20230328
- Source listing expiry
- 20271231
Source-listed ingredients
- NALOXEGOL OXALATE — 12.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (82625-8801-1) · 82625-8801-1
- 90 TABLET, FILM COATED in 1 BOTTLE (82625-8801-2) · 82625-8801-2
- 10 BLISTER PACK in 1 CARTON (82625-8801-3) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 82625-8801-3
- 1 BLISTER PACK in 1 CARTON (82625-8801-4) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 82625-8801-4
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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