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
- 80425-0501_2e738ab3-ae9a-9416-e063-6394a90afc75
- Product NDC
- 80425-0501
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250213
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, COATED in 1 BOTTLE (80425-0501-1) · 80425-0501-1
- 30 TABLET, COATED in 1 BOTTLE (80425-0501-2) · 80425-0501-2
- 60 TABLET, COATED in 1 BOTTLE (80425-0501-3) · 80425-0501-3
- 90 TABLET, COATED in 1 BOTTLE (80425-0501-4) · 80425-0501-4
- 120 TABLET, COATED in 1 BOTTLE (80425-0501-5) · 80425-0501-5
- 40 TABLET, COATED in 1 BOTTLE (80425-0501-6) · 80425-0501-6
- 180 TABLET, COATED in 1 BOTTLE (80425-0501-7) · 80425-0501-7
- 240 TABLET, COATED in 1 BOTTLE (80425-0501-8) · 80425-0501-8
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →