carafate

Generic: sucralfate

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name carafate
Generic Name sucralfate
Labeler allergan, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 58914-171
Product ID 58914-171_aa721873-bfcb-4428-8f2b-f40778d5cb86
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018333
Listing Expiration 2026-12-31
Marketing Start 1981-10-30

Pharmacologic Class

Established (EPC)
aluminum complex [epc]
Chemical Structure
organometallic compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58914171
Hyphenated Format 58914-171

Supplemental Identifiers

RxCUI
208097 314234
UNII
XX73205DH5
NUI
N0000175801 M0015420

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name carafate (source: ndc)
Generic Name sucralfate (source: ndc)
Application Number NDA018333 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (58914-171-10)
source: ndc

Packages (1)

58914-171-10 100 TABLET in 1 BOTTLE (58914-171-10)

Ingredients (1)

sucralfate (1 g/1)

Linked Drug Pages (1)

Carafate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aa721873-bfcb-4428-8f2b-f40778d5cb86", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["208097", "314234"], "spl_set_id": ["c87c6b50-6977-4fa7-ae98-40c0753f7aee"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58914-171-10)", "package_ndc": "58914-171-10", "marketing_start_date": "19811030"}], "brand_name": "Carafate", "product_id": "58914-171_aa721873-bfcb-4428-8f2b-f40778d5cb86", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "58914-171", "generic_name": "Sucralfate", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carafate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "NDA018333", "marketing_category": "NDA", "marketing_start_date": "19811030", "listing_expiration_date": "20261231"}