Package 31722-893-30

{"route": ["ORAL"], "spl_id": "47b1c419-e608-66b1-e063-6394a90ae253", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0331722894906", "0331722896306", "0331722894302", "0331722895309", "0331722893305", "0331722892902", "0331722895903", "0331722896900", "0331722892308", "0331722893909"], "unii": ["0J48LPH2TH", "864V2Q084H", "6M97XTV3HD"], "rxcui": ["999967", "999986", "999991", "999996", "1000001"], "spl_set_id": ["45e975ff-07b1-411a-96ee-a011d1619b1e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-893-30)", "package_ndc": "31722-893-30", "marketing_start_date": "20251006"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-893-32)  / 8 TABLET, FILM COATED in 1 BLISTER PACK (31722-893-31)", "package_ndc": "31722-893-32", "marketing_start_date": "20251006"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-893-90)", "package_ndc": "31722-893-90", "marketing_start_date": "20251006"}], "brand_name": "Olmesartan medoxomil, amlodipine and hydrochlorothiazide", "product_id": "31722-893_47b1c419-e608-66b1-e063-6394a90ae253", "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]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "31722-893", "generic_name": "Olmesartan medoxomil, amlodipine and hydrochlorothiazide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan medoxomil, amlodipine and hydrochlorothiazide", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA209242", "marketing_category": "ANDA", "marketing_start_date": "20251006", "listing_expiration_date": "20271231"}