Package 50090-7863-0

{"route": ["ORAL"], "spl_id": "d7534eb1-2b9b-45ea-a35d-f1653a807a91", "openfda": {"unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730869"], "spl_set_id": ["350c7317-a92d-4bcb-973f-19d6de87ed83"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7863-0)", "package_ndc": "50090-7863-0", "marketing_start_date": "20260122"}], "brand_name": "Amlodipine and Olmesartan Medoxomil", "product_id": "50090-7863_d7534eb1-2b9b-45ea-a35d-f1653a807a91", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50090-7863", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Olmesartan Medoxomil", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA206906", "marketing_category": "ANDA", "marketing_start_date": "20170515", "listing_expiration_date": "20271231"}