sucralfate

Generic: sucralfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2264
Product ID 72162-2264_9d3d9afa-c2ff-4182-90cf-861c34752ed8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074415
Listing Expiration 2026-12-31
Marketing Start 2020-02-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622264
Hyphenated Format 72162-2264

Supplemental Identifiers

RxCUI
314234
UNII
XX73205DH5
NUI
N0000175801 M0015420

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 sucralfate (source: ndc)
Generic Name sucralfate (source: ndc)
Application Number ANDA074415 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72162-2264-1)
  • 500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5)
source: ndc

Packages (2)

72162-2264-1 100 TABLET in 1 BOTTLE, PLASTIC (72162-2264-1) 72162-2264-5 500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5)

Ingredients (1)

sucralfate (1 g/1)

Linked Drug Pages (1)

Sucralfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9d3d9afa-c2ff-4182-90cf-861c34752ed8", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["28d7d257-8545-4b9f-8412-8ba144502400"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-2264-1)", "package_ndc": "72162-2264-1", "marketing_start_date": "20240223"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5)", "package_ndc": "72162-2264-5", "marketing_start_date": "20240223"}], "brand_name": "Sucralfate", "product_id": "72162-2264_9d3d9afa-c2ff-4182-90cf-861c34752ed8", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "72162-2264", "generic_name": "Sucralfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA074415", "marketing_category": "ANDA", "marketing_start_date": "20200217", "listing_expiration_date": "20261231"}