Package 68788-8946-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 68788-8946-1
Digits Only 6878889461
Product NDC 68788-8946
Product ID 68788-8946_6a99f537-9850-4eb9-8fbe-988cfcc728be
Description

100 TABLET in 1 BOTTLE (68788-8946-1)

Marketing

Marketing Status
Marketed Since 2015-10-28
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": "6a99f537-9850-4eb9-8fbe-988cfcc728be", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["5ec71444-cc55-47bd-8abc-b3cfc3b47d8e"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8946-1)", "package_ndc": "68788-8946-1", "marketing_start_date": "20151028"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8946-3)", "package_ndc": "68788-8946-3", "marketing_start_date": "20151028"}], "brand_name": "Sucralfate", "product_id": "68788-8946_6a99f537-9850-4eb9-8fbe-988cfcc728be", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68788-8946", "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": "ANDA070848", "marketing_category": "ANDA", "marketing_start_date": "20151027", "listing_expiration_date": "20261231"}