Package 70518-3293-2

{"route": ["ORAL"], "spl_id": "3a70fac1-8b78-477d-e063-6394a90a5c72", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["3a236293-35c1-4083-9805-ab40df535083"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3293-1)", "package_ndc": "70518-3293-1", "marketing_start_date": "20211230"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3293-2)", "package_ndc": "70518-3293-2", "marketing_start_date": "20220203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3293-3)", "package_ndc": "70518-3293-3", "marketing_start_date": "20220217"}], "brand_name": "Metoprolol Tartrate", "product_id": "70518-3293_3a70fac1-8b78-477d-e063-6394a90a5c72", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3293", "generic_name": "Metoprolol Tartrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20211213", "listing_expiration_date": "20261231"}