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United States· US:71335-2106_3e2312f9-2b0c-4137-88e2-5c75c659a6d0

OXYCODONE AND ACETAMINOPHEN

A medicinal product containing oxycodone hydrochloride; acetaminophen, registered in United States by Bryant Ranch Prepack.

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:71335-2106_3e2312f…PACKS LISTED18CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Manufacturer
Bryant Ranch Prepack
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 · 18

  • ndc11
    71335-2106-9
  • ndc11
    7133521061
    30 TABLET in 1 BOTTLE (71335-2106-1)
  • ndc11
    7133521062
    120 TABLET in 1 BOTTLE (71335-2106-2)
  • ndc11
    7133521063
    90 TABLET in 1 BOTTLE (71335-2106-3)
  • ndc11
    7133521064
    28 TABLET in 1 BOTTLE (71335-2106-4)
  • ndc11
    7133521065
    60 TABLET in 1 BOTTLE (71335-2106-5)
  • ndc11
    7133521066
    20 TABLET in 1 BOTTLE (71335-2106-6)
  • ndc11
    7133521067
    45 TABLET in 1 BOTTLE (71335-2106-7)
  • ndc11
    7133521068
    75 TABLET in 1 BOTTLE (71335-2106-8)
  • ndc11
    7133521069
    100 TABLET in 1 BOTTLE (71335-2106-9)
  • ndc11
    71335-2106-1
  • ndc11
    71335-2106-2
  • ndc11
    71335-2106-3
  • ndc11
    71335-2106-4
  • ndc11
    71335-2106-5
  • ndc11
    71335-2106-6
  • ndc11
    71335-2106-7
  • ndc11
    71335-2106-8

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/fba137b1-9043-4f1d-ac42-0e3801920738
GET /v1/drugs/fba137b1-9043-4f1d-ac42-0e3801920738?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": "10; 325",
  "substance": "OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN",
  "productndc": "71335-2106",
  "dosage_form": "TABLET",
  "dea_schedule": "CII",
  "strength_unit": "mg/1; mg/1",
  "application_number": "ANDA207419",
  "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.