Package 65862-559-10

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 65862-559-10
Digits Only 6586255910
Product NDC 65862-559
Description

10 BLISTER PACK in 1 CARTON (65862-559-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-09-28
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4784124c-9df4-42f6-8044-c0480c1a3bbf", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["7418f358-f536-4de6-adf0-562b4373f2e3"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-559-10)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "65862-559-10", "marketing_start_date": "20120928"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-90)", "package_ndc": "65862-559-90", "marketing_start_date": "20120928"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-99)", "package_ndc": "65862-559-99", "marketing_start_date": "20120928"}], "brand_name": "Pantoprazole Sodium", "product_id": "65862-559_4784124c-9df4-42f6-8044-c0480c1a3bbf", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "65862-559", "generic_name": "Pantoprazole Sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20271231"}