Package 0904-7470-72
Brand: sucralfate
Generic: sucralfate oral suspensionPackage Facts
Identity
Package NDC
0904-7470-72
Digits Only
0904747072
Product NDC
0904-7470
Description
100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)
Marketing
Marketing Status
Brand
sucralfate
Generic
sucralfate oral suspension
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "91b1db83-0f5e-4433-9104-6a2c315d13c8", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0309047470662"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["98a8fedd-fa06-416a-8a85-b899631978f9"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CUP, UNIT-DOSE in 1 CASE (0904-7470-01) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-01", "marketing_start_date": "20240626"}, {"sample": false, "description": "40 CUP, UNIT-DOSE in 1 CARTRIDGE (0904-7470-18) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-18", "marketing_start_date": "20240626"}, {"sample": false, "description": "20 CUP, UNIT-DOSE in 1 CASE (0904-7470-56) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-56", "marketing_start_date": "20240626"}, {"sample": false, "description": "10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-66", "marketing_start_date": "20240626"}, {"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (0904-7470-72) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-72", "marketing_start_date": "20240626"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (0904-7470-95) / 10 mL in 1 CUP, UNIT-DOSE (0904-7470-66)", "package_ndc": "0904-7470-95", "marketing_end_date": "20261031", "marketing_start_date": "20240626"}], "brand_name": "Sucralfate", "product_id": "0904-7470_91b1db83-0f5e-4433-9104-6a2c315d13c8", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0904-7470", "generic_name": "SUCRALFATE Oral Suspension", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA211884", "marketing_category": "ANDA", "marketing_start_date": "20240626", "listing_expiration_date": "20271231"}