Package 0904-6474-06

{"route": ["ORAL"], "spl_id": "349f9634-a35a-487f-acec-9148dba002cf", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["9c286e5c-2b36-422b-9f74-e8c0abb3f747"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6474-06)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6474-06", "marketing_start_date": "20260212"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6474-61)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0904-6474-61", "marketing_start_date": "20150601"}], "brand_name": "Pantoprazole Sodium", "product_id": "0904-6474_349f9634-a35a-487f-acec-9148dba002cf", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0904-6474", "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": "ANDA090074", "marketing_category": "ANDA", "marketing_start_date": "20150601", "listing_expiration_date": "20271231"}