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United States · US · US:76420-818_4ad5e40b-0272-c104-e063-6294a90a8237
Rabeprazole Sodium
Orange BookUNIISPLATC A02BC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeA02BC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11764208183030 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-30)
- ndc11764208186060 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-60)
- ndc11764208189090 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-90)
Annotations
UNII (FDA Substance ID)
3L36P16U4R
RABEPRAZOLE SODIUM
RxCUI 226868
Orange Book
A208644
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3L36P16U4R",
"rxcui": "226868",
"inchikey": "KRCQSTCYZUOBHN-UHFFFAOYSA-N",
"display_name": "RABEPRAZOLE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"4e8b9858-23a1-4363-b26f-ee6b9ff7ebf9": {
"match": "brand_token",
"title": "RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]",
"spl_version": "101",
"published_date": "2026-05-25"
}
},
"productid": "76420-818_4ad5e40b-0272-c104-e063-6294a90a8237",
"productndc": "76420-818",
"dosage_form": "TABLET, DELAYED RELEASE",
"orange_book": {
"appl_no": "208644",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "20MG",
"product_no": "001",
"approval_date": "Apr 24, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RABEPRAZOLE SODIUM",
"proprietary_name": "Rabeprazole Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208644",
"marketing_category": "ANDA",
"nonproprietary_name": "Rabeprazole Sodium",
"start_marketing_date": "20180427",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BC04.
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