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
- 76420-536_f4ca3781-8aec-9696-e053-2a95a90adf9f
- Product NDC
- 76420-536
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- TRAMADOL HYDROCHLORIDE
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140819
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-30) · 76420-536-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-60) · 76420-536-60
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-536-90) · 76420-536-90
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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