Package 72189-234-20

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 72189-234-20
Digits Only 7218923420
Product NDC 72189-234
Product ID 72189-234_2c285743-2fa6-4132-e063-6294a90adaff
Description

20 TABLET in 1 BOTTLE (72189-234-20)

Marketing

Marketing Status
Marketed Since 2021-06-18
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": "2c285743-2fa6-4132-e063-6294a90adaff", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["c50b5044-31ed-672a-e053-2995a90a49fc"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-234-20)", "package_ndc": "72189-234-20", "marketing_start_date": "20210618"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-234-90)", "package_ndc": "72189-234-90", "marketing_start_date": "20210618"}], "brand_name": "SUCRALFATE", "product_id": "72189-234_2c285743-2fa6-4132-e063-6294a90adaff", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "72189-234", "generic_name": "SUCRALFATE", "labeler_name": "DIRECT RX", "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": "20210618", "listing_expiration_date": "20261231"}