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United States · US · US:71335-1520_fd9976bd-f0c4-4e3a-b38b-2674f6e73c80

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 · 9

  • ndc11
    7133515201
    30 TABLET in 1 BOTTLE (71335-1520-1)
  • ndc11
    7133515202
    60 TABLET in 1 BOTTLE (71335-1520-2)
  • ndc11
    7133515203
    20 TABLET in 1 BOTTLE (71335-1520-3)
  • ndc11
    7133515204
    90 TABLET in 1 BOTTLE (71335-1520-4)
  • ndc11
    7133515205
    100 TABLET in 1 BOTTLE (71335-1520-5)
  • ndc11
    7133515206
    10 TABLET in 1 BOTTLE (71335-1520-6)
  • ndc11
    7133515207
    120 TABLET in 1 BOTTLE (71335-1520-7)
  • ndc11
    7133515208
    50 TABLET in 1 BOTTLE (71335-1520-8)
  • ndc11
    7133515209
    14 TABLET in 1 BOTTLE (71335-1520-9)

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A075805
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": "71335-1520_fd9976bd-f0c4-4e3a-b38b-2674f6e73c80",
  "productndc": "71335-1520",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "075805",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "Apr 16, 2001"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Apr 16, 2001"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "Famotidine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075805",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20010416",
  "active_numerator_strength": "20"
}

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