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
- 52817-195_bb37b29d-c827-d710-e053-2995a90acf1d
- Product NDC
- 52817-195
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- TRUPHARMA LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200901
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, COATED in 1 BOTTLE (52817-195-00) · 52817-195-00
- 100 TABLET, COATED in 1 BOTTLE (52817-195-10) · 52817-195-10
- 500 TABLET, COATED in 1 BOTTLE (52817-195-50) · 52817-195-50
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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