Package 70518-3987-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 70518-3987-1
Digits Only 7051839871
Product NDC 70518-3987
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-3987-1)

Marketing

Marketing Status
Marketed Since 2025-10-13
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": "4c5e4d36-4a3d-9acb-e063-6294a90aeb02", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["071cc50c-03cb-4a2e-8bbe-b04f3388cfed"], "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 BOTTLE, PLASTIC (70518-3987-1)", "package_ndc": "70518-3987-1", "marketing_start_date": "20251013"}], "brand_name": "Sucralfate", "product_id": "70518-3987_4c5e4d36-4a3d-9acb-e063-6294a90aeb02", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "70518-3987", "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": "NDA018333", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240118", "listing_expiration_date": "20271231"}