United States · FDA National Drug Code directory
Tramadol Hydrochloride
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
- 87063-117_4aea6bdc-3282-556d-e063-6394a90afb0c
- Product NDC
- 87063-117
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190809
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-01) · 87063-117-01
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-05) · 87063-117-05
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-10) · 87063-117-10
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-20) · 87063-117-20
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-30) · 87063-117-30
- 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-50) · 87063-117-50
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-60) · 87063-117-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-90) · 87063-117-90
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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