Package 80425-0085-3

Brand: pantoprazole sodium dr

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 80425-0085-3
Digits Only 8042500853
Product NDC 80425-0085
Product ID 80425-0085_2a98ff70-0367-7169-e063-6394a90adc74
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)

Marketing

Marketing Status
Marketed Since 2016-06-20
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": "2a98ff70-0367-7169-e063-6394a90adc74", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["b3277cb8-26d0-bce0-e053-2a95a90af6dd"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3)", "package_ndc": "80425-0085-3", "marketing_start_date": "20160620"}], "brand_name": "Pantoprazole Sodium DR", "product_id": "80425-0085_2a98ff70-0367-7169-e063-6394a90adc74", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "80425-0085", "generic_name": "Pantoprazole Sodium", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "brand_name_suffix": "DR", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA205119", "marketing_category": "ANDA", "marketing_start_date": "20160620", "listing_expiration_date": "20261231"}