Package 72162-2479-2

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 72162-2479-2
Digits Only 7216224792
Product NDC 72162-2479
Description

420 mL in 1 BOTTLE (72162-2479-2)

Marketing

Marketing Status
Marketed Since 2025-05-01
Brand sucralfate
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4e5200dd-dd65-48be-8dfd-e8411029de9b", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["abc44549-ac41-4aef-9b15-2ba536e1555f"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (72162-2479-2)", "package_ndc": "72162-2479-2", "marketing_start_date": "20250501"}], "brand_name": "sucralfate", "product_id": "72162-2479_4e5200dd-dd65-48be-8dfd-e8411029de9b", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "72162-2479", "generic_name": "Sucralfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216474", "marketing_category": "ANDA", "marketing_start_date": "20240710", "listing_expiration_date": "20261231"}