Package 58914-171-10

Brand: carafate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 58914-171-10
Digits Only 5891417110
Product NDC 58914-171
Product ID 58914-171_aa721873-bfcb-4428-8f2b-f40778d5cb86
Description

100 TABLET in 1 BOTTLE (58914-171-10)

Marketing

Marketing Status
Marketed Since 1981-10-30
Brand carafate
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Carafate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aa721873-bfcb-4428-8f2b-f40778d5cb86", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["208097", "314234"], "spl_set_id": ["c87c6b50-6977-4fa7-ae98-40c0753f7aee"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58914-171-10)", "package_ndc": "58914-171-10", "marketing_start_date": "19811030"}], "brand_name": "Carafate", "product_id": "58914-171_aa721873-bfcb-4428-8f2b-f40778d5cb86", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "58914-171", "generic_name": "Sucralfate", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carafate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "NDA018333", "marketing_category": "NDA", "marketing_start_date": "19811030", "listing_expiration_date": "20261231"}