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
- 55700-997_47fed614-6d8f-440b-af12-51ffa022167d
- Product NDC
- 55700-997
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Quality Care Products, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230207 / 20261130
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 (55700-997-01) · 55700-997-01
- 180 TABLET, COATED in 1 BOTTLE (55700-997-18) · 55700-997-18
- 30 TABLET, COATED in 1 BOTTLE (55700-997-30) · 55700-997-30
- 60 TABLET, COATED in 1 BOTTLE (55700-997-60) · 55700-997-60
- 90 TABLET, COATED in 1 BOTTLE (55700-997-90) · 55700-997-90
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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