Package 51655-527-83

{"route": ["ORAL"], "spl_id": "494dd968-14a0-24ee-e063-6294a90a5108", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["f319e981-81ff-22da-e053-2a95a90a2738"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-25)", "package_ndc": "51655-527-25", "marketing_start_date": "20221025"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-26)", "package_ndc": "51655-527-26", "marketing_start_date": "20220916"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-52)", "package_ndc": "51655-527-52", "marketing_start_date": "20221021"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-527-83)", "package_ndc": "51655-527-83", "marketing_start_date": "20230328"}], "brand_name": "Metoprolol Tartrate", "product_id": "51655-527_494dd968-14a0-24ee-e063-6294a90a5108", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51655-527", "generic_name": "Metoprolol Tartrate", "labeler_name": "Northwind Health Company, LLC", "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": "20220916", "listing_expiration_date": "20271231"}