Package 68071-3478-3

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 68071-3478-3
Digits Only 6807134783
Product NDC 68071-3478
Description

30 TABLET in 1 BOTTLE, PLASTIC (68071-3478-3)

Marketing

Marketing Status
Marketed Since 2023-08-03
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": "2ad411ea-6bf6-b3bd-e063-6394a90af2e7", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0368071347838"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["0206d7fa-a1d5-35d9-e063-6294a90a5eb3"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-3478-3)", "package_ndc": "68071-3478-3", "marketing_start_date": "20230803"}], "brand_name": "Sucralfate", "product_id": "68071-3478_2ad411ea-6bf6-b3bd-e063-6394a90af2e7", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68071-3478", "generic_name": "Sucralfate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}