sucralfate

Generic: sucralfate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sucralfate 1 g/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-429
Product ID 72189-429_2c4d741e-e60b-2e62-e063-6294a90a65fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074415
Listing Expiration 2026-12-31
Marketing Start 2023-03-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189429
Hyphenated Format 72189-429

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
  • 20 TABLET in 1 BOTTLE (72189-429-20)
  • 90 TABLET in 1 BOTTLE (72189-429-90)
source: ndc

Packages (2)

72189-429-20 20 TABLET in 1 BOTTLE (72189-429-20) 72189-429-90 90 TABLET in 1 BOTTLE (72189-429-90)

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": "2c4d741e-e60b-2e62-e063-6294a90a65fe", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["f5f0fecb-949c-3998-e053-2a95a90aac8c"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-429-20)", "package_ndc": "72189-429-20", "marketing_start_date": "20230302"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-429-90)", "package_ndc": "72189-429-90", "marketing_start_date": "20230302"}], "brand_name": "Sucralfate", "product_id": "72189-429_2c4d741e-e60b-2e62-e063-6294a90a65fe", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "72189-429", "generic_name": "Sucralfate", "labeler_name": "Direct_Rx", "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": "20230302", "listing_expiration_date": "20261231"}