United States · FDA National Drug Code directory

Nalocet

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
72245-193_585fcbf2-d16f-4eda-e063-6394a90a5965
Product NDC
72245-193
Form
TABLET
Composition / generic term
oxycodone and acetaminophen
Labeler
Forte Bio-Pharma LLC
Marketing category
ANDA
Marketing start / end (source format)
20180523
Source listing expiry
20271231

Source-listed ingredients

  • OXYCODONE HYDROCHLORIDE — 2.5 mg/1
  • ACETAMINOPHEN — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (72245-193-03) · 72245-193-03
  • 100 TABLET in 1 BOTTLE, PLASTIC (72245-193-10) · 72245-193-10

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.

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Nalocet — United States | Molindra Medicines