Package 82182-106-14

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 82182-106-14
Digits Only 8218210614
Product NDC 82182-106
Product ID 82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64
Description

420 mL in 1 BOTTLE (82182-106-14)

Marketing

Marketing Status
Marketed Since 2024-02-01
Brand sucralfate
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Sucralfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e171ec84-fb54-4598-a9e8-e37413ef2c64", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0382182106146"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["7407c58e-766f-4e93-a1bb-c77892ae0174"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Pacific Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (82182-106-14)", "package_ndc": "82182-106-14", "marketing_start_date": "20240201"}], "brand_name": "Sucralfate", "product_id": "82182-106_e171ec84-fb54-4598-a9e8-e37413ef2c64", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "82182-106", "generic_name": "Sucralfate", "labeler_name": "Pacific Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "NDA019183", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}