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United States· US:71335-1909_d5f709f5-ebb6-4ebc-a3d0-99463aaa8e0a

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:71335-1909_d5f709f…PACKS LISTED16CHECKEDSeptember 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 · 16

  • ndc11
    71335-1909-7
  • ndc11
    71335-1909-8
  • ndc11
    7133519091
    21 TABLET in 1 BOTTLE, PLASTIC (71335-1909-1)
  • ndc11
    7133519092
    36 TABLET in 1 BOTTLE, PLASTIC (71335-1909-2)
  • ndc11
    7133519093
    20 TABLET in 1 BOTTLE, PLASTIC (71335-1909-3)
  • ndc11
    7133519094
    30 TABLET in 1 BOTTLE, PLASTIC (71335-1909-4)
  • ndc11
    7133519095
    45 TABLET in 1 BOTTLE, PLASTIC (71335-1909-5)
  • ndc11
    7133519096
    60 TABLET in 1 BOTTLE, PLASTIC (71335-1909-6)
  • ndc11
    7133519097
    90 TABLET in 1 BOTTLE, PLASTIC (71335-1909-7)
  • ndc11
    7133519098
    120 TABLET in 1 BOTTLE, PLASTIC (71335-1909-8)
  • ndc11
    71335-1909-1
  • ndc11
    71335-1909-2
  • ndc11
    71335-1909-3
  • ndc11
    71335-1909-4
  • ndc11
    71335-1909-5
  • ndc11
    71335-1909-6

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/e257523e-ea17-4616-b349-2076b37538aa
GET /v1/drugs/e257523e-ea17-4616-b349-2076b37538aa?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": "71335-1909",
  "dosage_form": "TABLET",
  "dea_schedule": "CII",
  "strength_unit": "mg/1; mg/1",
  "application_number": "ANDA201278",
  "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.