Package 72865-230-10

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 72865-230-10
Digits Only 7286523010
Product NDC 72865-230
Product ID 72865-230_f26fc428-a419-1008-e053-2a95a90a83fc
Description

1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)

Marketing

Marketing Status
Marketed Since 2022-05-01
Brand pantoprazole sodium
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

PANTOPRAZOLE SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f26fc428-a419-1008-e053-2a95a90a83fc", "openfda": {"upc": ["0372865230107"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["17468dbf-84b6-4c53-9ad5-341350d2cfab"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)", "package_ndc": "72865-230-10", "marketing_start_date": "20220501"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)", "package_ndc": "72865-230-90", "marketing_start_date": "20220501"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72865-230_f26fc428-a419-1008-e053-2a95a90a83fc", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72865-230", "generic_name": "PANTOPRAZOLE", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20220501", "listing_expiration_date": "20261231"}