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
- 76420-105_b2ddcdd0-7229-99df-e053-2a95a90a8818
- Product NDC
- 76420-105
- Form
- TABLET, FILM COATED
- Composition / generic term
- TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121215
- 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, FILM COATED in 1 BOTTLE (76420-105-01) · 76420-105-01
- 2 TABLET, FILM COATED in 1 BOTTLE (76420-105-02) · 76420-105-02
- 3 TABLET, FILM COATED in 1 BOTTLE (76420-105-03) · 76420-105-03
- 10 TABLET, FILM COATED in 1 BOTTLE (76420-105-10) · 76420-105-10
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-105-30) · 76420-105-30
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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