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United States · US · US:72205-145_34acb853-6632-49cd-970a-e6fd840852d3

Famotidine

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerNovadoz Pharmaceuticals LLC
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7220514505
    500 TABLET, FILM COATED in 1 BOTTLE (72205-145-05)
  • ndc11
    7220514530
    30 TABLET, FILM COATED in 1 BOTTLE (72205-145-30)
  • ndc11
    7220514550
    50 TABLET, FILM COATED in 1 BOTTLE (72205-145-50)
  • ndc11
    7220514591
    100 TABLET, FILM COATED in 1 BOTTLE (72205-145-91)
  • ndc11
    7220514598
    75 TABLET, FILM COATED in 1 BOTTLE (72205-145-98)
  • ndc11
    7220514599
    1000 TABLET, FILM COATED in 1 BOTTLE (72205-145-99)

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A217400
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": "72205-145_34acb853-6632-49cd-970a-e6fd840852d3",
  "productndc": "72205-145",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "217400",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "Aug 6, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Aug 6, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "Famotidine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA217400",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20240806",
  "active_numerator_strength": "20"
}

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