Package 72162-2264-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 72162-2264-1
Digits Only 7216222641
Product NDC 72162-2264
Description

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

Marketing

Marketing Status
Marketed Since 2024-02-23
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": "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"}