Package 51655-031-52

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 51655-031-52
Digits Only 5165503152
Product NDC 51655-031
Product ID 51655-031_46ddb2f3-3673-237a-e063-6294a90aa52c
Description

30 TABLET in 1 BOTTLE, DISPENSING (51655-031-52)

Marketing

Marketing Status
Marketed Since 2015-02-09
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": "46ddb2f3-3673-237a-e063-6294a90aa52c", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["464bf611-4dbb-4707-b9dd-39ca178ed4bf"], "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, DISPENSING (51655-031-52)", "package_ndc": "51655-031-52", "marketing_start_date": "20150209"}], "brand_name": "Sucralfate", "product_id": "51655-031_46ddb2f3-3673-237a-e063-6294a90aa52c", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "51655-031", "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": "ANDA070848", "marketing_category": "ANDA", "marketing_start_date": "20150209", "listing_expiration_date": "20271231"}