Package 70518-3959-0

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 70518-3959-0
Digits Only 7051839590
Product NDC 70518-3959
Description

30 TABLET in 1 BLISTER PACK (70518-3959-0)

Marketing

Marketing Status
Marketed Since 2023-12-13
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": "3bb32136-21fc-131e-e063-6394a90ab24f", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["c0ee24dd-de9c-4d24-b8d8-c45b02752c1c"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3959-0)", "package_ndc": "70518-3959-0", "marketing_start_date": "20231213"}], "brand_name": "Sucralfate", "product_id": "70518-3959_3bb32136-21fc-131e-e063-6394a90ab24f", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "70518-3959", "generic_name": "Sucralfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215705", "marketing_category": "ANDA", "marketing_start_date": "20231213", "listing_expiration_date": "20261231"}