Sucralfate

Orange BookUNIISPLATC A02BX02

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeA02BX02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
7216222641
100 TABLET in 1 BOTTLE, PLASTIC (72162-2264-1)
ndc11
7216222645
500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5)

Annotations

UNII (FDA Substance ID)

XX73205DH5

SUCRALFATE

RxCUI 10156

Orange Book

A074415

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": "72162-2264_9d3d9afa-c2ff-4182-90cf-861c34752ed8",
  "productndc": "72162-2264",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "074415",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1GM",
        "product_no": "001",
        "approval_date": "Jun 8, 1998"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SUCRALFATE",
  "proprietary_name": "Sucralfate",
  "active_ingred_unit": "g/1",
  "application_number": "ANDA074415",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sucralfate",
  "start_marketing_date": "20200217",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code A02BX02.

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