Package 17856-0306-1

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 17856-0306-1
Digits Only 1785603061
Product NDC 17856-0306
Product ID 17856-0306_361f83ba-0caa-c1c1-e063-6394a90a4c10
Description

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1) / 10 mL in 1 CUP, UNIT-DOSE

Marketing

Marketing Status
Marketed Since 2023-08-10
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": "361f83ba-0caa-c1c1-e063-6394a90a4c10", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["e5073597-ac51-4e7c-a9dc-7695773a01f1"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1)  / 10 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-0306-1", "marketing_start_date": "20230810"}], "brand_name": "Sucralfate", "product_id": "17856-0306_361f83ba-0caa-c1c1-e063-6394a90a4c10", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "17856-0306", "generic_name": "Sucralfate", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA211884", "marketing_category": "ANDA", "marketing_start_date": "20220315", "listing_expiration_date": "20261231"}