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United States · US · US:0378-9205_107f926c-dcf7-4a04-a44a-e22ff1534f97
sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMylan Pharmaceuticals Inc.
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110378920535420 mL in 1 BOTTLE, PLASTIC (0378-9205-35)
Annotations
UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
A212913
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": "0378-9205_107f926c-dcf7-4a04-a44a-e22ff1534f97",
"productndc": "0378-9205",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "212913",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "1GM/10ML",
"product_no": "001",
"approval_date": "Sep 12, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SUCRALFATE",
"proprietary_name": "sucralfate",
"active_ingred_unit": "g/10mL",
"application_number": "ANDA212913",
"marketing_category": "ANDA",
"nonproprietary_name": "sucralfate",
"start_marketing_date": "20220922",
"active_numerator_strength": "1"
}Related drugs
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Access this data programmatically
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