Package 52817-840-16

Brand: sucralfate

Generic: sucralfate oral
NDC Package

Package Facts

Identity

Package NDC 52817-840-16
Digits Only 5281784016
Product NDC 52817-840
Description

473 mL in 1 BOTTLE (52817-840-16)

Marketing

Marketing Status
Marketed Since 2024-04-01
Brand sucralfate
Generic sucralfate oral
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4718799e-e742-c93e-e063-6294a90aacfd", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0352817840165"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["7d441128-45d2-4bf2-817b-665784992e90"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["TruPharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (52817-840-16)", "package_ndc": "52817-840-16", "marketing_start_date": "20240401"}], "brand_name": "Sucralfate", "product_id": "52817-840_4718799e-e742-c93e-e063-6294a90aacfd", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "52817-840", "generic_name": "Sucralfate Oral", "labeler_name": "TruPharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA213549", "marketing_category": "ANDA", "marketing_start_date": "20240401", "listing_expiration_date": "20261231"}