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United States · US · US:80425-0213_2a9a6113-0a2f-6005-e063-6294a90abc5e
Sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAdvanced Rx Pharmacy of Tennessee, LLC
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11804250213130 TABLET in 1 BOTTLE (80425-0213-1)
Annotations
UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
N018333
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "XX73205DH5",
"rxcui": "10156",
"inchikey": "IPLJAZDIICJQEL-JTJNLBSYSA-A",
"display_name": "SUCRALFATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"cd25eb96-29ea-48b2-bdee-c2ea98f216b8": {
"match": "brand_token",
"title": "SUCRALFATE TABLET [ASCLEMED USA INC.]",
"spl_version": "1",
"published_date": "2026-05-21"
}
},
"productid": "80425-0213_2a9a6113-0a2f-6005-e063-6294a90abc5e",
"productndc": "80425-0213",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "018333",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "1GM",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SUCRALFATE",
"proprietary_name": "Sucralfate",
"active_ingred_unit": "g/1",
"application_number": "NDA018333",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Sucralfate",
"start_marketing_date": "20230103",
"active_numerator_strength": "1"
}Related drugs
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