Package 82868-079-30

{"route": ["ORAL"], "spl_id": "4720215f-ae95-5f51-e063-6394a90ab4c2", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412"], "spl_set_id": ["47202157-3f32-275d-e063-6294a90a5c44"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-30)", "package_ndc": "82868-079-30", "marketing_start_date": "20250930"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-079-90)", "package_ndc": "82868-079-90", "marketing_start_date": "20250606"}], "brand_name": "Metoprolol Succinate", "product_id": "82868-079_4720215f-ae95-5f51-e063-6394a90ab4c2", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82868-079", "generic_name": "Metoprolol Succinate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20250606", "listing_expiration_date": "20261231"}