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
- 82804-114_2236031d-8596-4c21-8b16-83aa3e4122c1
- Product NDC
- 82804-114
- Form
- TABLET
- Composition / generic term
- tramadol hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180301
- 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 in 1 BOTTLE (82804-114-15) · 82804-114-15
- 20 TABLET in 1 BOTTLE (82804-114-20) · 82804-114-20
- 30 TABLET in 1 BOTTLE (82804-114-30) · 82804-114-30
- 40 TABLET in 1 BOTTLE (82804-114-40) · 82804-114-40
- 60 TABLET in 1 BOTTLE (82804-114-60) · 82804-114-60
- 240 TABLET in 1 BOTTLE (82804-114-64) · 82804-114-64
- 120 TABLET in 1 BOTTLE (82804-114-72) · 82804-114-72
- 180 TABLET in 1 BOTTLE (82804-114-78) · 82804-114-78
- 90 TABLET in 1 BOTTLE (82804-114-90) · 82804-114-90
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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