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United States · US · US:71335-1163_4ee49cc8-55ca-4274-9ea6-70d7891d8853

Buprenorphine HCl

Orange BookUNIISPLATC N07BC01

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN07BC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133511630
    120 TABLET in 1 BOTTLE (71335-1163-0)
  • ndc11
    7133511631
    90 TABLET in 1 BOTTLE (71335-1163-1)
  • ndc11
    7133511632
    60 TABLET in 1 BOTTLE (71335-1163-2)
  • ndc11
    7133511633
    30 TABLET in 1 BOTTLE (71335-1163-3)
  • ndc11
    7133511634
    20 TABLET in 1 BOTTLE (71335-1163-4)
  • ndc11
    7133511635
    7 TABLET in 1 BOTTLE (71335-1163-5)
  • ndc11
    7133511636
    28 TABLET in 1 BOTTLE (71335-1163-6)
  • ndc11
    7133511637
    1 TABLET in 1 BOTTLE (71335-1163-7)
  • ndc11
    7133511638
    12 TABLET in 1 BOTTLE (71335-1163-8)
  • ndc11
    7133511639
    14 TABLET in 1 BOTTLE (71335-1163-9)

Annotations

UNII (FDA Substance ID)
56W8MW3EN1
BUPRENORPHINE HYDROCHLORIDE
RxCUI 203841
Orange Book
A078633
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": "71335-1163_4ee49cc8-55ca-4274-9ea6-70d7891d8853",
  "productndc": "71335-1163",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "078633",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 2MG BASE",
        "product_no": "001",
        "approval_date": "Oct 8, 2009"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 8MG BASE",
        "product_no": "002",
        "approval_date": "Oct 8, 2009"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIII",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BUPRENORPHINE HYDROCHLORIDE",
  "proprietary_name": "Buprenorphine HCl",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078633",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Buprenorphine HCl",
  "start_marketing_date": "20091008",
  "active_numerator_strength": "8"
}

Related drugs

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