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
- 68071-4119_2d3fca70-2bc9-7bec-e063-6294a90a8da4
- Product NDC
- 68071-4119
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101115
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET, COATED in 1 BOTTLE (68071-4119-1) · 68071-4119-1
- 30 TABLET, COATED in 1 BOTTLE (68071-4119-3) · 68071-4119-3
- 40 TABLET, COATED in 1 BOTTLE (68071-4119-4) · 68071-4119-4
- 15 TABLET, COATED in 1 BOTTLE (68071-4119-5) · 68071-4119-5
- 60 TABLET, COATED in 1 BOTTLE (68071-4119-6) · 68071-4119-6
- 84 TABLET, COATED in 1 BOTTLE (68071-4119-7) · 68071-4119-7
- 180 TABLET, COATED in 1 BOTTLE (68071-4119-8) · 68071-4119-8
- 90 TABLET, COATED in 1 BOTTLE (68071-4119-9) · 68071-4119-9
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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