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United States · US · US:50090-5287_270e52df-d16b-4a96-b751-ff580c2f00c4
Sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500905287060 TABLET in 1 BOTTLE (50090-5287-0)
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": "50090-5287_270e52df-d16b-4a96-b751-ff580c2f00c4",
"productndc": "50090-5287",
"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": "20170925",
"active_numerator_strength": "1"
}Related drugs
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