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United States · US · US:71335-2981_3acfd469-5c34-4b0f-982f-77430ab099d6

Buprenorphine and Naloxone

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
    7133529810
    42 TABLET in 1 BOTTLE, PLASTIC (71335-2981-0)
  • ndc11
    7133529811
    30 TABLET in 1 BOTTLE, PLASTIC (71335-2981-1)
  • ndc11
    7133529812
    60 TABLET in 1 BOTTLE, PLASTIC (71335-2981-2)
  • ndc11
    7133529813
    90 TABLET in 1 BOTTLE, PLASTIC (71335-2981-3)
  • ndc11
    7133529814
    120 TABLET in 1 BOTTLE, PLASTIC (71335-2981-4)
  • ndc11
    7133529815
    14 TABLET in 1 BOTTLE, PLASTIC (71335-2981-5)
  • ndc11
    7133529816
    28 TABLET in 1 BOTTLE, PLASTIC (71335-2981-6)
  • ndc11
    7133529817
    6 TABLET in 1 BOTTLE, PLASTIC (71335-2981-7)
  • ndc11
    7133529818
    10 TABLET in 1 BOTTLE, PLASTIC (71335-2981-8)
  • ndc11
    7133529819
    21 TABLET in 1 BOTTLE, PLASTIC (71335-2981-9)

Annotations

UNII (FDA Substance ID)
56W8MW3EN1
BUPRENORPHINE HYDROCHLORIDE
RxCUI 203841
Orange Book
A205601
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": "71335-2981_3acfd469-5c34-4b0f-982f-77430ab099d6",
  "productndc": "71335-2981",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "205601",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 2MG BASE;EQ 0.5MG BASE",
        "product_no": "001",
        "approval_date": "Mar 30, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 8MG BASE;EQ 2MG BASE",
        "product_no": "002",
        "approval_date": "Mar 30, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE",
  "proprietary_name": "Buprenorphine and Naloxone",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "ANDA205601",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Buprenorphine and Naloxone",
  "start_marketing_date": "20200413",
  "active_numerator_strength": "8; 2"
}

Related drugs

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