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
63187-084_07437d1c-92eb-437a-8740-24a126006667
Product NDC
63187-084
Form
TABLET
Composition / generic term
Tramadol Hydrochloride and Acetaminophen
Labeler
Proficient Rx LP
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

  • 30 TABLET in 1 BOTTLE (63187-084-30) · 63187-084-30
  • 60 TABLET in 1 BOTTLE (63187-084-60) · 63187-084-60

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →