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United States · US · US:55910-814_3ffa405e-bc85-4614-afd0-7a8dfc288dad
dg health acid reducer
Orange BookUNIISPLATC A02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDolgencorp Inc
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1155910814711 BOTTLE in 1 CARTON (55910-814-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A077351
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": {
"5f0514bd-7893-4602-a17b-716fb9947572": {
"match": "brand_token",
"title": "DG HEALTH ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [DOLGENCORP INC]",
"spl_version": "9",
"published_date": "2026-02-10"
}
},
"productid": "55910-814_3ffa405e-bc85-4614-afd0-7a8dfc288dad",
"productndc": "55910-814",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "077351",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "20MG",
"product_no": "001",
"approval_date": "Sep 25, 2006"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FAMOTIDINE",
"proprietary_name": "dg health acid reducer",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077351",
"marketing_category": "ANDA",
"nonproprietary_name": "famotidine",
"start_marketing_date": "20220615",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BA03.
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