Package 50742-386-42

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 50742-386-42
Digits Only 5074238642
Product NDC 50742-386
Product ID 50742-386_03497f8d-e649-40bf-b5c9-2df985b0fab4
Description

420 mL in 1 BOTTLE (50742-386-42)

Marketing

Marketing Status
Discontinued 2026-07-31
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": "03497f8d-e649-40bf-b5c9-2df985b0fab4", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["1921b3fc-f55c-e503-e063-6394a90a7da9"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (50742-386-42)", "package_ndc": "50742-386-42", "marketing_end_date": "20260731", "marketing_start_date": "20241121"}], "brand_name": "Sucralfate", "product_id": "50742-386_03497f8d-e649-40bf-b5c9-2df985b0fab4", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "50742-386", "generic_name": "Sucralfate", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216726", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20241121"}