Package 69238-2676-1

{"route": ["ORAL"], "spl_id": "31d0d1f2-a0c7-4cd3-80d2-d9f231687adc", "openfda": {"upc": ["0369238267617", "0369238267518", "0369238267310", "0369238267419"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["02f9b562-6f7f-4783-bb0d-67c318073e1c"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69238-2676-1)", "package_ndc": "69238-2676-1", "marketing_start_date": "20181203"}], "brand_name": "Amlodipine and Olmesartan Medoxomil", "product_id": "69238-2676_31d0d1f2-a0c7-4cd3-80d2-d9f231687adc", "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": "69238-2676", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "Amneal Pharmaceuticals NY LLC", "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": "40 mg/1"}], "application_number": "ANDA209010", "marketing_category": "ANDA", "marketing_start_date": "20181203", "listing_expiration_date": "20261231"}