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United States · US · US:57896-317_2875fd94-dabd-960e-e063-6394a90a623c
Famotidine
Orange BookUNIISPLATC A02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGERI-CARE PHARMACEUTICAL CORP
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1157896317031 BOTTLE in 1 CARTON (57896-317-03) / 30 TABLET, FILM COATED in 1 BOTTLE
- ndc1157896317061 BOTTLE in 1 CARTON (57896-317-06) / 60 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A215822
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": "57896-317_2875fd94-dabd-960e-e063-6394a90a623c",
"productndc": "57896-317",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "215822",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Jan 28, 2022"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "20MG",
"product_no": "002",
"approval_date": "Jan 28, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FAMOTIDINE",
"proprietary_name": "Famotidine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA215822",
"marketing_category": "ANDA",
"nonproprietary_name": "Famotidine",
"start_marketing_date": "20240301",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code A02BA03.
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