United States · FDA National Drug Code directory
TAPENTADOL
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
- 0054-0937_7fef46e2-c049-44d8-962f-fdd233dad041
- Product NDC
- 0054-0937
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Tapentadol Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20251215
- Source listing expiry
- 20271231
Source-listed ingredients
- TAPENTADOL HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0937-21) · 0054-0937-21
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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