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United States · US · US:82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64
Sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPacific Pharma, Inc.
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118218210614420 mL in 1 BOTTLE (82182-106-14)
Annotations
UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
N019183
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": "82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64",
"productndc": "82182-106",
"dosage_form": "SUSPENSION",
"orange_book": {
"appl_no": "019183",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "1GM/10ML",
"product_no": "001",
"approval_date": "Dec 16, 1993"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SUCRALFATE",
"proprietary_name": "Sucralfate",
"active_ingred_unit": "g/10mL",
"application_number": "NDA019183",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Sucralfate",
"start_marketing_date": "20240201",
"active_numerator_strength": "1"
}Related drugs
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