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United States · US · US:68788-8946_6a99f537-9850-4eb9-8fbe-988cfcc728be
Sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPreferred Pharmaceuticals Inc.
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc116878889461100 TABLET in 1 BOTTLE (68788-8946-1)
- ndc11687888946330 TABLET in 1 BOTTLE (68788-8946-3)
Annotations
UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
A070848
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": "68788-8946_6a99f537-9850-4eb9-8fbe-988cfcc728be",
"productndc": "68788-8946",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "070848",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1GM",
"product_no": "001",
"approval_date": "Mar 29, 1996"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SUCRALFATE",
"proprietary_name": "Sucralfate",
"active_ingred_unit": "g/1",
"application_number": "ANDA070848",
"marketing_category": "ANDA",
"nonproprietary_name": "Sucralfate",
"start_marketing_date": "20151027",
"active_numerator_strength": "1"
}Related drugs
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