Package 0615-4517-39

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 0615-4517-39
Digits Only 0615451739
Product NDC 0615-4517
Product ID 0615-4517_7226b7de-1569-4e22-9ed3-1de5487e68ed
Description

30 TABLET in 1 BLISTER PACK (0615-4517-39)

Marketing

Marketing Status
Marketed Since 2010-01-08
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": "7226b7de-1569-4e22-9ed3-1de5487e68ed", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["d67dcaad-56c1-4e77-a0c8-655970808414"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-4517-39)", "package_ndc": "0615-4517-39", "marketing_start_date": "20100108"}], "brand_name": "Sucralfate", "product_id": "0615-4517_7226b7de-1569-4e22-9ed3-1de5487e68ed", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0615-4517", "generic_name": "Sucralfate", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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": "19961111", "listing_expiration_date": "20261231"}