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United States· US:70518-3862_422983e3-7c40-32e6-e063-6294a90ae95d

buprenorphine hydrochloride and naloxone hydrochloride dihydrate

A oripavine derivatives product containing buprenorphine hydrochloride and naloxone hydrochloride dihydrate, registered in United States by REMEDYREPACK INC..

ATC N02AEOrange BookUS 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…normalisedbuprenorphine hydrochloride and nalox…ATCN02AEREGISTER NO.US:70518-3862_422983e…PACKS LISTED1CHECKEDJune 3, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Manufacturer
REMEDYREPACK INC.
Country
United States (US)
ATC code
N02AE
ATC class
Oripavine derivatives
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
June 3, 2026

Packs & prices · 1

  • ndc11
    7051838620
    30 TABLET in 1 BLISTER PACK (70518-3862-0)

Regulatory notes

UNII (FDA substance ID)
56W8MW3EN1
BUPRENORPHINE HYDROCHLORIDE
RxCUI 203841
Orange Book
A203326
ABAB
DailyMed SPL labels
1 version tracked

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/f78dc2ca-3370-4593-ac99-a05603951c1b
GET /v1/drugs/f78dc2ca-3370-4593-ac99-a05603951c1b?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.

{
  "unii": {
    "unii": "56W8MW3EN1",
    "rxcui": "203841",
    "inchikey": "UAIXRPCCYXNJMQ-RZIPZOSSSA-N",
    "display_name": "BUPRENORPHINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "spl_meta": {
    "2738feae-316e-426f-971c-5f142ac01b60": {
      "match": "brand_token",
      "title": "BUPRENORPHINE PATCH [RHODES PHARMACEUTICALS LLC]",
      "spl_version": "17",
      "published_date": "2026-06-01"
    }
  },
  "productid": "70518-3862_422983e3-7c40-32e6-e063-6294a90ae95d",
  "productndc": "70518-3862",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "203326",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 2MG BASE;EQ 0.5MG BASE",
        "product_no": "001",
        "approval_date": "Jun 27, 2014"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 8MG BASE;EQ 2MG BASE",
        "product_no": "002",
        "approval_date": "Jun 27, 2014"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE",
  "proprietary_name": "buprenorphine hydrochloride and naloxone hydrochloride dihydrate",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "ANDA203326",
  "marketing_category": "ANDA",
  "nonproprietary_name": "buprenorphine hydrochloride and naloxone hydrochloride dihydrate",
  "start_marketing_date": "20230915",
  "active_numerator_strength": "2; .5"
}

See everything about buprenorphine hydrochloride and naloxone hydrochloride dihydrate.

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.