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United States · US · US:87063-176_52122b7a-f718-404c-e063-6394a90a6daf
Sucralfate
Orange BookUNIISPLATC A02BX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerASCLEMED USA INC.
CountryUS (United States)
ATC codeA02BX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc118706317601100 TABLET in 1 BOTTLE (87063-176-01)
- ndc118706317605500 TABLET in 1 BOTTLE (87063-176-05)
- ndc118706317612120 TABLET in 1 BOTTLE (87063-176-12)
- ndc11870631763030 TABLET in 1 BOTTLE (87063-176-30)
- ndc11870631766060 TABLET in 1 BOTTLE (87063-176-60)
- ndc11870631769090 TABLET in 1 BOTTLE (87063-176-90)
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": "87063-176_52122b7a-f718-404c-e063-6394a90a6daf",
"productndc": "87063-176",
"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": "19961111",
"active_numerator_strength": "1"
}Related drugs
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