Package 51655-475-52
Brand: sucralfate
Generic: sucralfatePackage Facts
Identity
Package NDC
51655-475-52
Digits Only
5165547552
Product NDC
51655-475
Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-475-52)
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": "490f38ea-fc45-7aa2-e063-6294a90a9f1c", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["f3095db3-fd02-873c-e053-2a95a90a5b1f"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-475-52)", "package_ndc": "51655-475-52", "marketing_start_date": "20201118"}], "brand_name": "Sucralfate", "product_id": "51655-475_490f38ea-fc45-7aa2-e063-6294a90a9f1c", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "51655-475", "generic_name": "Sucralfate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "NDA018333", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20201118", "listing_expiration_date": "20271231"}