Package 0904-6870-45
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
0904-6870-45
Digits Only
0904687045
Product NDC
0904-6870
Description
80 BLISTER PACK in 1 CARTON (0904-6870-45) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Marketing
Marketing Status
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": "7f8bdcaa-2a4b-4ed0-a649-a528b3b278a6", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["de419aa0-caa9-40fb-bc6d-e341c94273c7"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "80 BLISTER PACK in 1 CARTON (0904-6870-45) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6870-45", "marketing_start_date": "20120928"}], "brand_name": "Pantoprazole Sodium", "product_id": "0904-6870_7f8bdcaa-2a4b-4ed0-a649-a528b3b278a6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0904-6870", "generic_name": "Pantoprazole Sodium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20271231"}