Back to search
🇺🇸

United States · US · US:71335-0409_d24aad6a-0ce6-45d1-a84a-2e738c497bb2

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
    7133504090
    40 TABLET in 1 BOTTLE (71335-0409-0)
  • ndc11
    7133504091
    30 TABLET in 1 BOTTLE (71335-0409-1)
  • ndc11
    7133504092
    60 TABLET in 1 BOTTLE (71335-0409-2)
  • ndc11
    7133504093
    20 TABLET in 1 BOTTLE (71335-0409-3)
  • ndc11
    7133504094
    90 TABLET in 1 BOTTLE (71335-0409-4)
  • ndc11
    7133504095
    100 TABLET in 1 BOTTLE (71335-0409-5)
  • ndc11
    7133504096
    10 TABLET in 1 BOTTLE (71335-0409-6)
  • ndc11
    7133504097
    120 TABLET in 1 BOTTLE (71335-0409-7)
  • ndc11
    7133504098
    50 TABLET in 1 BOTTLE (71335-0409-8)
  • ndc11
    7133504099
    14 TABLET in 1 BOTTLE (71335-0409-9)

Annotations

UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A078916
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": "71335-0409_d24aad6a-0ce6-45d1-a84a-2e738c497bb2",
  "productndc": "71335-0409",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "078916",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "001",
        "approval_date": "May 22, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "May 22, 2009"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FAMOTIDINE",
  "proprietary_name": "Famotidine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078916",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Famotidine",
  "start_marketing_date": "20160129",
  "active_numerator_strength": "20"
}

Related drugs

Other records sharing ATC code A02BA03.

Access this data programmatically

Query Famotidine 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.