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United States · US · US:71335-2805_b2d70cef-4104-46d3-af20-aec60436b34b

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 · 10

  • ndc11
    7133528050
    40 TABLET, FILM COATED in 1 BOTTLE (71335-2805-0)
  • ndc11
    7133528051
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2805-1)
  • ndc11
    7133528052
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2805-2)
  • ndc11
    7133528053
    20 TABLET, FILM COATED in 1 BOTTLE (71335-2805-3)
  • ndc11
    7133528054
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2805-4)
  • ndc11
    7133528055
    100 TABLET, FILM COATED in 1 BOTTLE (71335-2805-5)
  • ndc11
    7133528056
    10 TABLET, FILM COATED in 1 BOTTLE (71335-2805-6)
  • ndc11
    7133528057
    120 TABLET, FILM COATED in 1 BOTTLE (71335-2805-7)
  • ndc11
    7133528058
    50 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8)
  • ndc11
    7133528059
    14 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9)

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": "71335-2805_b2d70cef-4104-46d3-af20-aec60436b34b",
  "productndc": "71335-2805",
  "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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