Package 68071-3812-3

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 68071-3812-3
Digits Only 6807138123
Product NDC 68071-3812
Product ID 68071-3812_31a7e09b-5fe1-f1fc-e063-6394a90a63d9
Description

30 TABLET in 1 BOTTLE (68071-3812-3)

Marketing

Marketing Status
Marketed Since 2025-03-19
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": "31a7e09b-5fe1-f1fc-e063-6394a90a63d9", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0368071381238"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["31a7dcd0-e677-249a-e063-6294a90a75f6"], "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 (68071-3812-3)", "package_ndc": "68071-3812-3", "marketing_start_date": "20250319"}], "brand_name": "Sucralfate", "product_id": "68071-3812_31a7e09b-5fe1-f1fc-e063-6394a90a63d9", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "68071-3812", "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": "ANDA215705", "marketing_category": "ANDA", "marketing_start_date": "20230520", "listing_expiration_date": "20261231"}