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United States · US · US:51407-683_22941e23-59e9-f792-e063-6394a90a2552

Famotidine

Orange BookUNIISPLATC A02BA03

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

Identification

ManufacturerGolden State Medical Supply, Inc.
CountryUS (United States)
ATC codeA02BA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    5140768310
    36 BOTTLE in 1 BOX (51407-683-10) / 1000 TABLET in 1 BOTTLE
  • ndc11
    5140768318
    36 BOTTLE in 1 BOX (51407-683-18) / 180 TABLET in 1 BOTTLE
  • ndc11
    5140768325
    36 BOTTLE in 1 BOX (51407-683-25) / 25 TABLET in 1 BOTTLE
  • ndc11
    5140768330
    36 BOTTLE in 1 BOX (51407-683-30) / 30 TABLET in 1 BOTTLE
  • ndc11
    5140768350
    36 BOTTLE in 1 BOX (51407-683-50) / 50 TABLET in 1 BOTTLE
  • ndc11
    5140768390
    36 BOTTLE in 1 BOX (51407-683-90) / 90 TABLET in 1 BOTTLE

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": "51407-683_22941e23-59e9-f792-e063-6394a90a2552",
  "productndc": "51407-683",
  "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"
}

Related drugs

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