Package 70756-018-51

{"route": ["ORAL"], "spl_id": "2c507c43-c033-4b6e-b954-f0f2fb617289", "openfda": {"upc": ["0370756019121", "0370756019909"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["0502f935-af7a-4f1e-8c3e-29e20647c885"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (70756-018-51)", "package_ndc": "70756-018-51", "marketing_start_date": "20240425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-018-90)", "package_ndc": "70756-018-90", "marketing_start_date": "20240425"}], "brand_name": "Pantoprazole sodium delayed-release", "product_id": "70756-018_2c507c43-c033-4b6e-b954-f0f2fb617289", "dosage_form": "TABLET", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70756-018", "generic_name": "Pantoprazole sodium delayed-release", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole sodium delayed-release", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA215880", "marketing_category": "ANDA", "marketing_start_date": "20240425", "listing_expiration_date": "20261231"}