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United States · US · US:71335-0370_337a85de-6910-03aa-e063-6294a90a2e71

Famotidine

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA02BA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 8

  • ndc11
    7133503701
    30 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1)
  • ndc11
    7133503702
    60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)
  • ndc11
    7133503703
    20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)
  • ndc11
    7133503704
    90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)
  • ndc11
    7133503705
    100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)
  • ndc11
    7133503706
    10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)
  • ndc11
    7133503707
    120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)
  • ndc11
    7133503708
    50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A206530
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5QZO15J2Z8",
    "rxcui": "4278",
    "inchikey": "XUFQPHANEAPEMJ-UHFFFAOYSA-N",
    "display_name": "FAMOTIDINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "e53928f3-5181-490b-acfb-be8d4cea60a9": {
      "match": "brand_token",
      "title": "FAMOTIDINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-0370_337a85de-6910-03aa-e063-6294a90a2e71",
  "productndc": "71335-0370",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "206530",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "Dec 22, 2015"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Dec 22, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "Famotidine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA206530",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20151222",
  "active_numerator_strength": "20"
}

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