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
- 67296-1834_4387f592-853f-01ea-e063-6394a90a6a4f
- Product NDC
- 67296-1834
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- RedPharm Drug Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210422
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, COATED in 1 BOTTLE (67296-1834-1) · 67296-1834-1
- 20 TABLET, COATED in 1 BOTTLE (67296-1834-2) · 67296-1834-2
- 30 TABLET, COATED in 1 BOTTLE (67296-1834-3) · 67296-1834-3
- 40 TABLET, COATED in 1 BOTTLE (67296-1834-4) · 67296-1834-4
- 6 TABLET, COATED in 1 BOTTLE (67296-1834-6) · 67296-1834-6
- 15 TABLET, COATED in 1 BOTTLE (67296-1834-7) · 67296-1834-7
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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