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United States · US · US:63629-1307_fc785200-389b-e031-e053-6294a90a88f1

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
    6362913070
    28 TABLET in 1 BOTTLE (63629-1307-0)
  • ndc11
    6362913071
    100 TABLET in 1 BOTTLE (63629-1307-1)
  • ndc11
    6362913072
    60 TABLET in 1 BOTTLE (63629-1307-2)
  • ndc11
    6362913073
    30 TABLET in 1 BOTTLE (63629-1307-3)
  • ndc11
    6362913074
    20 TABLET in 1 BOTTLE (63629-1307-4)
  • ndc11
    6362913076
    150 TABLET in 1 BOTTLE (63629-1307-6)
  • ndc11
    6362913077
    90 TABLET in 1 BOTTLE (63629-1307-7)
  • ndc11
    6362913078
    40 TABLET in 1 BOTTLE (63629-1307-8)
  • ndc11
    6362913079
    120 TABLET in 1 BOTTLE (63629-1307-9)

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": "63629-1307_fc785200-389b-e031-e053-6294a90a88f1",
  "productndc": "63629-1307",
  "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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