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United States· US:65162-207_34daf86b-3616-4e9e-a43e-56666cf95fa4

Oxycodone and Acetaminophen

A medicinal product containing oxycodone hydrochloride; acetaminophen, registered in United States by Amneal Pharmaceuticals LLC.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedOxycodone and AcetaminophenATC—REGISTER NO.US:65162-207_34daf86b…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Manufacturer
Amneal Pharmaceuticals LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 6

  • ndc11
    65162-207-03
  • ndc11
    65162-207-10
  • ndc11
    65162-207-50
  • ndc11
    6516220703
    30 TABLET in 1 BOTTLE (65162-207-03)
  • ndc11
    6516220710
    100 TABLET in 1 BOTTLE (65162-207-10)
  • ndc11
    6516220750
    500 TABLET in 1 BOTTLE (65162-207-50)

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Oxycodone hydrochloride; acetaminophen in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All oxycodone hydrochloride; acetaminophen products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Greece · Oxycodone Paracetamol Rafarm
  • Italy · Depalgos

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/cb3b32f5-d1b3-4694-80a0-dd8a097f2511
GET /v1/drugs/cb3b32f5-d1b3-4694-80a0-dd8a097f2511?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "7.5; 325",
  "substance": "OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN",
  "productndc": "65162-207",
  "dosage_form": "TABLET",
  "dea_schedule": "CII",
  "strength_unit": "mg/1; mg/1",
  "application_number": "ANDA040778",
  "marketing_category": "ANDA"
}

See everything about oxycodone hydrochloride; acetaminophen.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.