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United States · US · US:71335-1858_9bc52e26-1d52-4d68-894a-d3b300f5f090

BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE

Orange BookUNIISPLATC N02AE

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN02AE
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133518580
    42 TABLET in 1 BOTTLE, PLASTIC (71335-1858-0)
  • ndc11
    7133518581
    30 TABLET in 1 BOTTLE, PLASTIC (71335-1858-1)
  • ndc11
    7133518582
    60 TABLET in 1 BOTTLE, PLASTIC (71335-1858-2)
  • ndc11
    7133518583
    90 TABLET in 1 BOTTLE, PLASTIC (71335-1858-3)
  • ndc11
    7133518584
    120 TABLET in 1 BOTTLE, PLASTIC (71335-1858-4)
  • ndc11
    7133518585
    14 TABLET in 1 BOTTLE, PLASTIC (71335-1858-5)
  • ndc11
    7133518586
    28 TABLET in 1 BOTTLE, PLASTIC (71335-1858-6)
  • ndc11
    7133518587
    6 TABLET in 1 BOTTLE, PLASTIC (71335-1858-7)
  • ndc11
    7133518588
    10 TABLET in 1 BOTTLE, PLASTIC (71335-1858-8)
  • ndc11
    7133518589
    21 TABLET in 1 BOTTLE, PLASTIC (71335-1858-9)

Annotations

UNII (FDA Substance ID)
56W8MW3EN1
BUPRENORPHINE HYDROCHLORIDE
RxCUI 203841
Orange Book
A209069
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "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": "71335-1858_9bc52e26-1d52-4d68-894a-d3b300f5f090",
  "productndc": "71335-1858",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "209069",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 2MG BASE;EQ 0.5MG BASE",
        "product_no": "001",
        "approval_date": "Jul 17, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 8MG BASE;EQ 2MG BASE",
        "product_no": "002",
        "approval_date": "Jul 17, 2020"
      }
    ],
    "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": "ANDA209069",
  "marketing_category": "ANDA",
  "nonproprietary_name": "BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE",
  "start_marketing_date": "20210122",
  "active_numerator_strength": "8; 2"
}

Related drugs

Other records sharing ATC code N02AE.

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