Package 0093-2210-98

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 0093-2210-98
Digits Only 0093221098
Product NDC 0093-2210
Product ID 0093-2210_c363786b-0fde-45c0-9575-2a4ca71aa592
Description

90 TABLET in 1 BOTTLE (0093-2210-98)

Marketing

Marketing Status
Marketed Since 2011-01-12
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": "c363786b-0fde-45c0-9575-2a4ca71aa592", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0300932210981"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["c7a43df7-eb37-4273-9250-87953b1fd270"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2210-01)", "package_ndc": "0093-2210-01", "marketing_start_date": "19961111"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-2210-05)", "package_ndc": "0093-2210-05", "marketing_start_date": "19961111"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0093-2210-98)", "package_ndc": "0093-2210-98", "marketing_start_date": "20110112"}], "brand_name": "Sucralfate", "product_id": "0093-2210_c363786b-0fde-45c0-9575-2a4ca71aa592", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0093-2210", "generic_name": "Sucralfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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"}