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United States · US · US:11822-6123_e53e617d-7619-49d4-8e1a-b0f7b3f04288
acid relief
Orange BookUNIISPLATC A02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRite Aid Corporation
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111822612301 BOTTLE in 1 CARTON (11822-6123-0) / 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": {
"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": "11822-6123_e53e617d-7619-49d4-8e1a-b0f7b3f04288",
"productndc": "11822-6123",
"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": "acid relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077351",
"marketing_category": "ANDA",
"nonproprietary_name": "famotidine",
"start_marketing_date": "20230719",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BA03.
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