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
- 68071-3644_23aab36b-87f1-4569-e063-6394a90aae17
- Product NDC
- 68071-3644
- Form
- TABLET
- Composition / generic term
- tramadol hydrochloride
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 30 TABLET in 1 PACKAGE (68071-3644-3) · 68071-3644-3
- 40 TABLET in 1 PACKAGE (68071-3644-4) · 68071-3644-4
- 15 TABLET in 1 PACKAGE (68071-3644-5) · 68071-3644-5
- 60 TABLET in 1 PACKAGE (68071-3644-6) · 68071-3644-6
- 90 TABLET in 1 PACKAGE (68071-3644-9) · 68071-3644-9
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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