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United States · US · US:58914-170_cb835be9-f4ba-47c4-b1db-d2f731371432

Carafate

Orange BookUNIISPLATC A02BX02

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

Identification

ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeA02BX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    5891417014
    420 mL in 1 BOTTLE (58914-170-14)
  • ndc11
    5891417060
    6 CUP, UNIT-DOSE in 1 BOX (58914-170-60) / 10 mL in 1 CUP, UNIT-DOSE

Annotations

UNII (FDA Substance ID)
XX73205DH5
SUCRALFATE
RxCUI 10156
Orange Book
N019183
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": {
    "c87c6b50-6977-4fa7-ae98-40c0753f7aee": {
      "match": "brand_token",
      "title": "CARAFATE (SUCRALFATE) TABLET [ALLERGAN, INC.]",
      "spl_version": "17",
      "published_date": "2025-11-17"
    }
  },
  "productid": "58914-170_cb835be9-f4ba-47c4-b1db-d2f731371432",
  "productndc": "58914-170",
  "dosage_form": "SUSPENSION",
  "orange_book": {
    "appl_no": "019183",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "1GM/10ML",
        "product_no": "001",
        "approval_date": "Dec 16, 1993"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "SUCRALFATE",
  "proprietary_name": "Carafate",
  "active_ingred_unit": "g/10mL",
  "application_number": "NDA019183",
  "marketing_category": "NDA",
  "nonproprietary_name": "Sucralfate",
  "start_marketing_date": "19931216",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code A02BX02.

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