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 SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 58914-170
Product ID 58914-170_cb835be9-f4ba-47c4-b1db-d2f731371432
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019183
Listing Expiration 2026-12-31
Marketing Start 1993-12-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58914170
Hyphenated Format 58914-170

Supplemental Identifiers

RxCUI
208094 313123
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 NDA019183 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 420 mL in 1 BOTTLE (58914-170-14)
  • 6 CUP, UNIT-DOSE in 1 BOX (58914-170-60) / 10 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (2)

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

Ingredients (1)

sucralfate (1 g/10mL)

Linked Drug Pages (1)

Carafate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cb835be9-f4ba-47c4-b1db-d2f731371432", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["208094", "313123"], "spl_set_id": ["0fb67b1c-b4c0-46f2-8a81-df1510e006aa"], "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": "420 mL in 1 BOTTLE (58914-170-14)", "package_ndc": "58914-170-14", "marketing_start_date": "19931216"}, {"sample": true, "description": "6 CUP, UNIT-DOSE in 1 BOX (58914-170-60)  / 10 mL in 1 CUP, UNIT-DOSE", "package_ndc": "58914-170-60", "marketing_start_date": "19931216"}], "brand_name": "Carafate", "product_id": "58914-170_cb835be9-f4ba-47c4-b1db-d2f731371432", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "58914-170", "generic_name": "Sucralfate", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carafate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "NDA019183", "marketing_category": "NDA", "marketing_start_date": "19931216", "listing_expiration_date": "20261231"}