Package 72189-514-30
Brand: pantoprazole sodium dr
Generic: pantoprazole sodium drPackage Facts
Identity
Package NDC
72189-514-30
Digits Only
7218951430
Product NDC
72189-514
Description
30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-30)
Marketing
Marketing Status
Brand
pantoprazole sodium dr
Generic
pantoprazole sodium dr
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c4adb93-e6cf-6f33-e063-6294a90a063b", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["0515ceaa-7d17-c92f-e063-6294a90a044e"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-30)", "package_ndc": "72189-514-30", "marketing_start_date": "20230911"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-90)", "package_ndc": "72189-514-90", "marketing_start_date": "20230911"}], "brand_name": "Pantoprazole Sodium DR", "product_id": "72189-514_4c4adb93-e6cf-6f33-e063-6294a90a063b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-514", "generic_name": "Pantoprazole Sodium DR", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium DR", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20271231"}