Package 50268-745-14

Brand: sucralfate

Generic: sucralfate oral
NDC Package

Package Facts

Identity

Package NDC 50268-745-14
Digits Only 5026874514
Product NDC 50268-745
Description

40 CUP in 1 BOX (50268-745-14) / 10 mL in 1 CUP (50268-745-11)

Marketing

Marketing Status
Marketed Since 2022-08-31
Brand sucralfate
Generic sucralfate oral
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4510a8c1-2007-1ac1-e063-6294a90a1375", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["e78ef7d4-faa7-aebf-e053-2995a90a6f84"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 CUP in 1 BOX (50268-745-14)  / 10 mL in 1 CUP (50268-745-11)", "package_ndc": "50268-745-14", "marketing_start_date": "20220831"}], "brand_name": "Sucralfate", "product_id": "50268-745_4510a8c1-2007-1ac1-e063-6294a90a1375", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "50268-745", "generic_name": "Sucralfate Oral", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA209356", "marketing_category": "ANDA", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}