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United States · US · US:67091-244_70bc7062-ab3c-43eb-b524-0d8c6d1a674d
Acid Reducer
Orange BookUNIISPLATC A02BA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWinCo Foods, LLC
CountryUS (United States)
ATC codeA02BA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1167091244301 BOTTLE in 1 CARTON (67091-244-30) / 30 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
BK76465IHM
RANITIDINE HYDROCHLORIDE
RxCUI 203136
Orange Book
A201745
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "BK76465IHM",
"rxcui": "203136",
"inchikey": "GGWBHVILAJZWKJ-UHFFFAOYSA-N",
"display_name": "RANITIDINE HYDROCHLORIDE",
"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": "67091-244_70bc7062-ab3c-43eb-b524-0d8c6d1a674d",
"productndc": "67091-244",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "201745",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 75MG BASE",
"product_no": "001",
"approval_date": "Feb 29, 2012"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "RANITIDINE HYDROCHLORIDE",
"proprietary_name": "Acid Reducer",
"active_ingred_unit": "mg/1",
"application_number": "ANDA201745",
"marketing_category": "ANDA",
"nonproprietary_name": "Ranitidine Hydrochloride",
"start_marketing_date": "20120802",
"active_numerator_strength": "75"
}Related drugs
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- GBGavilast 75mg tabletsReckitt Benckiser Healthcare (UK) Ltd
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