Package 80425-0162-1

Brand: pantoprazole sodium dr

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 80425-0162-1
Digits Only 8042501621
Product NDC 80425-0162
Product ID 80425-0162_2a99a670-af2e-299d-e063-6294a90a05d2
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-1)

Marketing

Marketing Status
Marketed Since 2014-09-10
Brand pantoprazole sodium dr
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Pantoprazole Sodium DR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a99a670-af2e-299d-e063-6294a90a05d2", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["c89a5396-1d94-c7fa-e053-2995a90a9063"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-1)", "package_ndc": "80425-0162-1", "marketing_start_date": "20140910"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-2)", "package_ndc": "80425-0162-2", "marketing_start_date": "20140910"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-3)", "package_ndc": "80425-0162-3", "marketing_start_date": "20140910"}], "brand_name": "Pantoprazole Sodium DR", "product_id": "80425-0162_2a99a670-af2e-299d-e063-6294a90a05d2", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0162", "generic_name": "Pantoprazole Sodium", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "brand_name_suffix": "DR", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}