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
- 80425-0588_552e6399-c3c3-d362-e063-6394a90a0f8f
- Product NDC
- 80425-0588
- Form
- TABLET
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260626
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (80425-0588-1) · 80425-0588-1
- 30 TABLET in 1 BOTTLE (80425-0588-2) · 80425-0588-2
- 40 TABLET in 1 BOTTLE (80425-0588-3) · 80425-0588-3
- 60 TABLET in 1 BOTTLE (80425-0588-4) · 80425-0588-4
- 90 TABLET in 1 BOTTLE (80425-0588-5) · 80425-0588-5
- 120 TABLET in 1 BOTTLE (80425-0588-6) · 80425-0588-6
- 180 TABLET in 1 BOTTLE (80425-0588-7) · 80425-0588-7
- 240 TABLET in 1 BOTTLE (80425-0588-8) · 80425-0588-8
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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