Package 80425-0091-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 80425-0091-1
Digits Only 8042500911
Product NDC 80425-0091
Product ID 80425-0091_2a994dc6-72f5-0559-e063-6394a90a0ecf
Description

30 TABLET in 1 BOTTLE (80425-0091-1)

Marketing

Marketing Status
Marketed Since 1996-11-11
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": "2a994dc6-72f5-0559-e063-6394a90a0ecf", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["b39f22c8-f224-451a-e053-2995a90aaad7"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0091-1)", "package_ndc": "80425-0091-1", "marketing_start_date": "19961111"}], "brand_name": "Sucralfate", "product_id": "80425-0091_2a994dc6-72f5-0559-e063-6394a90a0ecf", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "80425-0091", "generic_name": "Sucralfate", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA070848", "marketing_category": "ANDA", "marketing_start_date": "19961111", "listing_expiration_date": "20261231"}