United States · FDA National Drug Code directory
Tramadol Hydrochloride and Acetaminophen
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
- 76420-983_d5db9e70-d7a4-462d-e053-2995a90a32be
- Product NDC
- 76420-983
- Form
- TABLET
- Composition / generic term
- Tramadol Hydrochloride and Acetaminophen
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091217
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 37.5 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TABLET in 1 BOTTLE (76420-983-01) · 76420-983-01
- 2 TABLET in 1 BOTTLE (76420-983-02) · 76420-983-02
- 3 TABLET in 1 BOTTLE (76420-983-03) · 76420-983-03
- 10 TABLET in 1 BOTTLE (76420-983-10) · 76420-983-10
- 30 TABLET in 1 BOTTLE (76420-983-30) · 76420-983-30
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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