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
- 72189-311_2c3cf1d7-38f5-4d25-e063-6294a90aa8cd
- Product NDC
- 72189-311
- Form
- TABLET, COATED
- Composition / generic term
- TRAMADOL HYDROCHLORIDE
- Labeler
- DirectRx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220112
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 TABLET, COATED in 1 BOTTLE (72189-311-12) · 72189-311-12
- 20 TABLET, COATED in 1 BOTTLE (72189-311-20) · 72189-311-20
- 30 TABLET, COATED in 1 BOTTLE (72189-311-30) · 72189-311-30
- 40 TABLET, COATED in 1 BOTTLE (72189-311-40) · 72189-311-40
- 60 TABLET, COATED in 1 BOTTLE (72189-311-60) · 72189-311-60
- 120 TABLET, COATED in 1 BOTTLE (72189-311-72) · 72189-311-72
- 180 TABLET, COATED in 1 BOTTLE (72189-311-82) · 72189-311-82
- 240 TABLET, COATED in 1 BOTTLE (72189-311-84) · 72189-311-84
- 90 TABLET, COATED in 1 BOTTLE (72189-311-90) · 72189-311-90
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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