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United States · US · US:21130-023_53be867e-a578-91cd-9f9d-a0bec097a4ae
Famotidine
Orange BookUNIISPLATC A02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlbertsons Companies
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1121130023251 BOTTLE in 1 CARTON (21130-023-25) / 25 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A077367
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": "21130-023_53be867e-a578-91cd-9f9d-a0bec097a4ae",
"productndc": "21130-023",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "077367",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "20MG",
"product_no": "001",
"approval_date": "Sep 25, 2006"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "002",
"approval_date": "Aug 17, 2001"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FAMOTIDINE",
"proprietary_name": "Famotidine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077367",
"marketing_category": "ANDA",
"nonproprietary_name": "Famotidine",
"start_marketing_date": "20211101",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BA03.
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