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United States · US · US:42507-141_d614f778-d1b8-4fa4-94f8-59978dfbfb52
acid reducer
Orange BookUNIISPLATC A02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHyVee Inc
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1142507141751 BOTTLE in 1 CARTON (42507-141-75) / 90 TABLET, FILM COATED in 1 BOTTLE (42507-141-90)
Annotations
UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A075400
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": {
"9826dd26-5592-4f96-9274-005ef9462cb4": {
"match": "brand_token",
"title": "ACID RELIEF (FAMOTIDINE) TABLET, FILM COATED [RITE AID CORPORATION]",
"spl_version": "5",
"published_date": "2026-05-28"
}
},
"productid": "42507-141_d614f778-d1b8-4fa4-94f8-59978dfbfb52",
"productndc": "42507-141",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075400",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Mar 18, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FAMOTIDINE",
"proprietary_name": "acid reducer",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075400",
"marketing_category": "ANDA",
"nonproprietary_name": "Famotidine",
"start_marketing_date": "20091019",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code A02BA03.
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