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United States · US · US:71335-2114_fc506a9a-8d99-f22b-e053-6394a90ad6d9

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
    7133521140
    28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0)
  • ndc11
    7133521141
    100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1)
  • ndc11
    7133521142
    60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2)
  • ndc11
    7133521143
    30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3)
  • ndc11
    7133521144
    20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4)
  • ndc11
    7133521146
    150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6)
  • ndc11
    7133521147
    90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7)
  • ndc11
    7133521148
    40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8)
  • ndc11
    7133521149
    120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9)

Annotations

UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
A074415
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": "71335-2114_fc506a9a-8d99-f22b-e053-6394a90ad6d9",
  "productndc": "71335-2114",
  "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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