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
- 50090-5789_d2130333-f392-4f3c-b988-c4147c6c9595
- Product NDC
- 50090-5789
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190809
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-5789-0) · 50090-5789-0
- 20 TABLET, FILM COATED in 1 BOTTLE (50090-5789-1) · 50090-5789-1
- 50 TABLET, FILM COATED in 1 BOTTLE (50090-5789-2) · 50090-5789-2
- 15 TABLET, FILM COATED in 1 BOTTLE (50090-5789-4) · 50090-5789-4
- 60 TABLET, FILM COATED in 1 BOTTLE (50090-5789-5) · 50090-5789-5
- 120 TABLET, FILM COATED in 1 BOTTLE (50090-5789-9) · 50090-5789-9
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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