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
- 60219-2348_12ec39ff-7a96-4467-a778-7537868c0ccd
- Product NDC
- 60219-2348
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230213
- 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, COATED in 1 BOTTLE (60219-2348-1) · 60219-2348-1
- 10 TABLET, COATED in 1 BOTTLE (60219-2348-4) · 60219-2348-4
- 500 TABLET, COATED in 1 BOTTLE (60219-2348-5) · 60219-2348-5
- 1000 TABLET, COATED in 1 BOTTLE (60219-2348-7) · 60219-2348-7
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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