Package 42291-936-90

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 42291-936-90
Digits Only 4229193690
Product NDC 42291-936
Description

90 TABLET in 1 BOTTLE (42291-936-90)

Marketing

Marketing Status
Marketed Since 2023-10-31
Brand sucralfate
Generic sucralfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c0e47e-08b1-0c73-e063-6394a90a90b7", "openfda": {"nui": ["N0000175801", "M0015420"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["0909acc5-c746-17fb-e063-6394a90a677f"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-936-90)", "package_ndc": "42291-936-90", "marketing_start_date": "20231031"}], "brand_name": "Sucralfate", "product_id": "42291-936_48c0e47e-08b1-0c73-e063-6394a90a90b7", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "42291-936", "generic_name": "Sucralfate", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA215576", "marketing_category": "ANDA", "marketing_start_date": "20231031", "listing_expiration_date": "20271231"}