Package 54738-005-42
Brand: sucralfate
Generic: sucralfatePackage Facts
Identity
Package NDC
54738-005-42
Digits Only
5473800542
Product NDC
54738-005
Description
420 mL in 1 BOTTLE (54738-005-42)
Marketing
Marketing Status
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": "35d366c4-22fb-2cca-e063-6394a90a6980", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["7ac10c3f-9d50-4702-900c-41075ac6f896"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Richmond Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (54738-005-42)", "package_ndc": "54738-005-42", "marketing_start_date": "20250522"}], "brand_name": "Sucralfate", "product_id": "54738-005_35d366c4-22fb-2cca-e063-6394a90a6980", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "54738-005", "generic_name": "Sucralfate", "labeler_name": "Richmond Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216726", "marketing_category": "ANDA", "marketing_start_date": "20241121", "listing_expiration_date": "20261231"}