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United States · US · US:0904-7470_91b1db83-0f5e-4433-9104-6a2c315d13c8

Sucralfate

Orange BookUNIISPLATC A02BX02

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

Identification

ManufacturerMajor Pharmaceuticals
CountryUS (United States)
ATC codeA02BX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    0904747001
    30 CUP, UNIT-DOSE in 1 CASE (0904-7470-01) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • ndc11
    0904747018
    40 CUP, UNIT-DOSE in 1 CARTRIDGE (0904-7470-18) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • ndc11
    0904747056
    20 CUP, UNIT-DOSE in 1 CASE (0904-7470-56) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • ndc11
    0904747066
    10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • ndc11
    0904747072
    100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
  • ndc11
    0904747095
    50 CUP, UNIT-DOSE in 1 CASE (0904-7470-95) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)

Annotations

UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
A211884
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": "0904-7470_91b1db83-0f5e-4433-9104-6a2c315d13c8",
  "productndc": "0904-7470",
  "dosage_form": "SUSPENSION",
  "orange_book": {
    "appl_no": "211884",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1GM/10ML",
        "product_no": "001",
        "approval_date": "Mar 15, 2022"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SUCRALFATE",
  "proprietary_name": "Sucralfate",
  "active_ingred_unit": "g/10mL",
  "application_number": "ANDA211884",
  "marketing_category": "ANDA",
  "nonproprietary_name": "SUCRALFATE Oral Suspension",
  "start_marketing_date": "20240626",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code A02BX02.

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