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United States · US · US:0093-2210_c363786b-0fde-45c0-9575-2a4ca71aa592

Sucralfate

Orange BookUNIISPLATC A02BX02

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeA02BX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    0093221001
    100 TABLET in 1 BOTTLE (0093-2210-01)
  • ndc11
    0093221005
    500 TABLET in 1 BOTTLE (0093-2210-05)
  • ndc11
    0093221098
    90 TABLET in 1 BOTTLE (0093-2210-98)

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": "0093-2210_c363786b-0fde-45c0-9575-2a4ca71aa592",
  "productndc": "0093-2210",
  "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

Other records sharing ATC code A02BX02.

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