Package 82804-102-30

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 82804-102-30
Digits Only 8280410230
Product NDC 82804-102
Description

30 TABLET in 1 BOTTLE, PLASTIC (82804-102-30)

Marketing

Marketing Status
Marketed Since 2024-05-06
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": "51459cdb-a04a-49c2-8ee4-8f234f522476", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0382804102303"], "unii": ["XX73205DH5"], "rxcui": ["314234"], "spl_set_id": ["51459cdb-a04a-49c2-8ee4-8f234f522476"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82804-102-30)", "package_ndc": "82804-102-30", "marketing_start_date": "20240506"}], "brand_name": "Sucralfate", "product_id": "82804-102_51459cdb-a04a-49c2-8ee4-8f234f522476", "dosage_form": "TABLET", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "82804-102", "generic_name": "Sucralfate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/1"}], "application_number": "ANDA074415", "marketing_category": "ANDA", "marketing_start_date": "20200217", "listing_expiration_date": "20261231"}