Sucralfate

Orange BookUNIISPLATC A02BX02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerREMEDYREPACK INC.

CountryUS (United States)

ATC codeA02BX02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
7051807750
30 TABLET in 1 BLISTER PACK (70518-0775-0)
ndc11
7051807752
30 TABLET in 1 BLISTER PACK (70518-0775-2)

Annotations

UNII (FDA Substance ID)

XX73205DH5

SUCRALFATE

RxCUI 10156

Orange Book

A070848

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": "70518-0775_4837097f-8d0b-9280-e063-6394a90ab409",
  "productndc": "70518-0775",
  "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": "20171010",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code A02BX02.

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