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United States · US · US:71335-2637_dc7f253b-f40a-4774-8456-1d383fb35b0c

Sucralfate

Orange BookUNIISPLATC A02BX02

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeA02BX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    7133526370
    28 TABLET in 1 BOTTLE (71335-2637-0)
  • ndc11
    7133526371
    100 TABLET in 1 BOTTLE (71335-2637-1)
  • ndc11
    7133526372
    60 TABLET in 1 BOTTLE (71335-2637-2)
  • ndc11
    7133526373
    30 TABLET in 1 BOTTLE (71335-2637-3)
  • ndc11
    7133526374
    20 TABLET in 1 BOTTLE (71335-2637-4)
  • ndc11
    7133526376
    150 TABLET in 1 BOTTLE (71335-2637-6)
  • ndc11
    7133526377
    90 TABLET in 1 BOTTLE (71335-2637-7)
  • ndc11
    7133526378
    40 TABLET in 1 BOTTLE (71335-2637-8)
  • ndc11
    7133526379
    120 TABLET in 1 BOTTLE (71335-2637-9)

Annotations

UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
N018333
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": "71335-2637_dc7f253b-f40a-4774-8456-1d383fb35b0c",
  "productndc": "71335-2637",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "018333",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "1GM",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SUCRALFATE",
  "proprietary_name": "Sucralfate",
  "active_ingred_unit": "g/1",
  "application_number": "NDA018333",
  "marketing_category": "NDA AUTHORIZED GENERIC",
  "nonproprietary_name": "Sucralfate",
  "start_marketing_date": "20170925",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code A02BX02.

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