Back to search
🇺🇸

United States · US · US:71335-2062_ab44332a-6f04-4f07-8209-e472206d5707

NALTREXONE HYDROCHLORIDE

Orange BookUNIISPLATC N07BB04

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN07BB04
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7133520621
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1)
  • ndc11
    7133520622
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2)
  • ndc11
    7133520623
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3)
  • ndc11
    7133520624
    45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4)
  • ndc11
    7133520625
    120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5)
  • ndc11
    7133520626
    15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6)

Annotations

UNII (FDA Substance ID)
Z6375YW9SF
NALTREXONE HYDROCHLORIDE
RxCUI 105069
Orange Book
A090356
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "Z6375YW9SF",
    "rxcui": "105069",
    "inchikey": "RHBRMCOKKKZVRY-ITLPAZOVSA-N",
    "display_name": "NALTREXONE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "fa0b0881-97f3-4ca2-bc15-0954293081db": {
      "match": "brand_token",
      "title": "NALTREXONE HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK]",
      "spl_version": "13",
      "published_date": "2026-05-20"
    }
  },
  "productid": "71335-2062_ab44332a-6f04-4f07-8209-e472206d5707",
  "productndc": "71335-2062",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "090356",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Feb 24, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NALTREXONE HYDROCHLORIDE",
  "proprietary_name": "NALTREXONE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA090356",
  "marketing_category": "ANDA",
  "nonproprietary_name": "NALTREXONE HYDROCHLORIDE",
  "start_marketing_date": "20120229",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code N07BB04.

Access this data programmatically

Query NALTREXONE HYDROCHLORIDE and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.