Package 72205-001-30

{"route": ["ORAL"], "spl_id": "79a88ea4-ddf4-4ee9-acc2-91047ce636d5", "openfda": {"upc": ["0372205001312", "0372205001053"], "unii": ["B8956S8609"], "rxcui": ["311787"], "spl_set_id": ["04e0936f-2248-48e4-8031-ac6ccc2df294"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72205-001-05)", "package_ndc": "72205-001-05", "marketing_start_date": "20190416"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-001-30)", "package_ndc": "72205-001-30", "marketing_start_date": "20190416"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (72205-001-31)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-001-11)", "package_ndc": "72205-001-31", "marketing_start_date": "20190416"}], "brand_name": "Moxifloxacin Hydrochloride Tablets, 400 mg", "product_id": "72205-001_79a88ea4-ddf4-4ee9-acc2-91047ce636d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Quinolone Antimicrobial [EPC]", "Quinolones [CS]"], "product_ndc": "72205-001", "generic_name": "Moxifloxacin Hydrochloride Tablets, 400 mg", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Moxifloxacin Hydrochloride Tablets, 400 mg", "active_ingredients": [{"name": "MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE", "strength": "400 mg/1"}], "application_number": "ANDA208682", "marketing_category": "ANDA", "marketing_start_date": "20180721", "listing_expiration_date": "20261231"}