Package 63629-9153-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 63629-9153-1
Digits Only 6362991531
Product NDC 63629-9153
Description

500 TABLET in 1 BOTTLE, PLASTIC (63629-9153-1)

Marketing

Marketing Status
Marketed Since 2022-01-26
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": "b0edecc4-682e-4bfe-8d0e-25234fef06c0", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["25ae2ebc-a7e0-4fc9-a8d1-07f7dd7138e5"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (63629-9153-1)", "package_ndc": "63629-9153-1", "marketing_start_date": "20220126"}], "brand_name": "Sucralfate", "product_id": "63629-9153_b0edecc4-682e-4bfe-8d0e-25234fef06c0", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "63629-9153", "generic_name": "Sucralfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA074415", "marketing_category": "ANDA", "marketing_start_date": "20200217", "listing_expiration_date": "20261231"}