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
- 76420-733_3c537239-67e9-1101-e063-6394a90a397f
- Product NDC
- 76420-733
- Form
- TABLET, COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230724
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, COATED in 1 BOTTLE (76420-733-00) · 76420-733-00
- 100 TABLET, COATED in 1 BOTTLE (76420-733-01) · 76420-733-01
- 2 TABLET, COATED in 1 BOTTLE (76420-733-02) · 76420-733-02
- 500 TABLET, COATED in 1 BOTTLE (76420-733-05) · 76420-733-05
- 1 TABLET, COATED in 1 BOTTLE (76420-733-10) · 76420-733-10
- 120 TABLET, COATED in 1 BOTTLE (76420-733-12) · 76420-733-12
- 30 TABLET, COATED in 1 BOTTLE (76420-733-30) · 76420-733-30
- 60 TABLET, COATED in 1 BOTTLE (76420-733-60) · 76420-733-60
- 90 TABLET, COATED in 1 BOTTLE (76420-733-90) · 76420-733-90
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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