Package 67296-2147-4

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 67296-2147-4
Digits Only 6729621474
Product NDC 67296-2147
Product ID 67296-2147_4637f5d7-c529-1d00-e063-6394a90a754f
Description

40 TABLET in 1 BOTTLE (67296-2147-4)

Marketing

Marketing Status
Marketed Since 2023-05-20
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": "4637f5d7-c529-1d00-e063-6394a90a754f", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["3251e156-4c52-63b3-e063-6294a90a9a95"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET in 1 BOTTLE (67296-2147-4)", "package_ndc": "67296-2147-4", "marketing_start_date": "20230520"}], "brand_name": "Sucralfate", "product_id": "67296-2147_4637f5d7-c529-1d00-e063-6394a90a754f", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "67296-2147", "generic_name": "Sucralfate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215705", "marketing_category": "ANDA", "marketing_start_date": "20230520", "listing_expiration_date": "20261231"}