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United States · US · US:58602-729_81d45120-49d4-4de8-8477-79312e2c1d56
Acid Reducer
In shortageOrange BookUNIISPLATC A02BC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAurohealth LLC
CountryUS (United States)
ATC codeA02BC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc1158602729011 BLISTER PACK in 1 CARTON (58602-729-01) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- ndc1158602729022 BLISTER PACK in 1 CARTON (58602-729-02) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- ndc1158602729033 BLISTER PACK in 1 CARTON (58602-729-03) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
- ndc1158602729051 BOTTLE in 1 CARTON (58602-729-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- ndc1158602729612 BOTTLE in 1 CARTON (58602-729-61) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- ndc1158602729623 BOTTLE in 1 CARTON (58602-729-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
- ndc1158602729652 BLISTER PACK in 1 CARTON (58602-729-65) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58602-729-64)
Annotations
UNII (FDA Substance ID)
426QFE7XLK
OMEPRAZOLE MAGNESIUM
RxCUI 236486
Orange Book
A206877
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Omeprazole Delayed Release Capsule
Raw payload (JSON)
{
"unii": {
"unii": "426QFE7XLK",
"rxcui": "236486",
"inchikey": "KWORUUGOSLYAGD-UHFFFAOYSA-N",
"display_name": "OMEPRAZOLE MAGNESIUM",
"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": "58602-729_81d45120-49d4-4de8-8477-79312e2c1d56",
"productndc": "58602-729",
"dosage_form": "TABLET, DELAYED RELEASE",
"orange_book": {
"appl_no": "206877",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 20MG BASE",
"product_no": "001",
"approval_date": "Jun 6, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OMEPRAZOLE MAGNESIUM",
"shortage_reason": "Omeprazole Delayed Release Capsule",
"shortage_status": "current",
"proprietary_name": "Acid Reducer",
"active_ingred_unit": "mg/1",
"application_number": "ANDA206877",
"marketing_category": "ANDA",
"nonproprietary_name": "Omeprazole",
"start_marketing_date": "20180606",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BC01.
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