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United States · US · US:50742-386_03497f8d-e649-40bf-b5c9-2df985b0fab4
Sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerIngenus Pharmaceuticals, LLC
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc115074238642420 mL in 1 BOTTLE (50742-386-42)
Annotations
UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
A216726
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": "50742-386_03497f8d-e649-40bf-b5c9-2df985b0fab4",
"productndc": "50742-386",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "216726",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1GM/10ML",
"product_no": "001",
"approval_date": "Mar 21, 2024"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SUCRALFATE",
"proprietary_name": "Sucralfate",
"active_ingred_unit": "g/10mL",
"application_number": "ANDA216726",
"marketing_category": "ANDA",
"nonproprietary_name": "Sucralfate",
"start_marketing_date": "20241121",
"active_numerator_strength": "1"
}Related drugs
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