Package 68788-8779-9

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 68788-8779-9
Digits Only 6878887799
Product NDC 68788-8779
Description

100 TABLET in 1 BOTTLE (68788-8779-9)

Marketing

Marketing Status
Marketed Since 2024-12-10
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": "657d271c-f93e-4356-a043-e8c383b4a023", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["a434bf8f-cc60-4d84-a9a4-61c3ff6b700e"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8779-3)", "package_ndc": "68788-8779-3", "marketing_start_date": "20241210"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8779-9)", "package_ndc": "68788-8779-9", "marketing_start_date": "20241210"}], "brand_name": "Sucralfate", "product_id": "68788-8779_657d271c-f93e-4356-a043-e8c383b4a023", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68788-8779", "generic_name": "Sucralfate", "labeler_name": "Preferred Pharmaceuticals 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": "20241210", "listing_expiration_date": "20271231"}