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
- 71205-740_39d70777-2751-4f9e-a26b-675027a634c6
- Product NDC
- 71205-740
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200923
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (71205-740-15) · 71205-740-15
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-740-20) · 71205-740-20
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-740-30) · 71205-740-30
- 40 TABLET, FILM COATED in 1 BOTTLE (71205-740-40) · 71205-740-40
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-740-60) · 71205-740-60
- 120 TABLET, FILM COATED in 1 BOTTLE (71205-740-72) · 71205-740-72
- 180 TABLET, FILM COATED in 1 BOTTLE (71205-740-78) · 71205-740-78
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-740-90) · 71205-740-90
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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