Package 67046-1469-3

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 67046-1469-3
Digits Only 6704614693
Product NDC 67046-1469
Description

30 TABLET in 1 BLISTER PACK (67046-1469-3)

Marketing

Marketing Status
Marketed Since 2025-02-04
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": "2d5893c4-5f80-adea-e063-6294a90ae3e9", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["2d586736-73ae-9af0-e063-6294a90ad875"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1469-3)", "package_ndc": "67046-1469-3", "marketing_start_date": "20250204"}], "brand_name": "Sucralfate", "product_id": "67046-1469_2d5893c4-5f80-adea-e063-6294a90ae3e9", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "67046-1469", "generic_name": "Sucralfate", "labeler_name": "Coupler LLC", "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": "20250204", "listing_expiration_date": "20261231"}