Package 0713-0791-75

Brand: sucralfate

Generic: sucralfate
NDC Package

Package Facts

Identity

Package NDC 0713-0791-75
Digits Only 0713079175
Product NDC 0713-0791
Description

420 mL in 1 BOTTLE (0713-0791-75)

Marketing

Marketing Status
Marketed Since 2024-12-19
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": "27c19a55-ceb8-91c3-e063-6394a90a726e", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0307130791755"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["3054ce94-78a2-4da4-8b14-95311b412ab2"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Cosette Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE (0713-0791-75)", "package_ndc": "0713-0791-75", "marketing_start_date": "20241219"}], "brand_name": "Sucralfate", "product_id": "0713-0791_27c19a55-ceb8-91c3-e063-6394a90a726e", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "0713-0791", "generic_name": "Sucralfate", "labeler_name": "Cosette Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA217126", "marketing_category": "ANDA", "marketing_start_date": "20241219", "listing_expiration_date": "20261231"}