Package 76420-030-30

{"route": ["ORAL"], "spl_id": "e4ec0115-3fdf-8c05-e053-2995a90a8353", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["751f0d33-ceff-40b0-9329-9125f176e06a"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-030-01)", "package_ndc": "76420-030-01", "marketing_start_date": "20200619"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76420-030-05)", "package_ndc": "76420-030-05", "marketing_start_date": "20200619"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (76420-030-12)", "package_ndc": "76420-030-12", "marketing_start_date": "20220729"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-030-30)", "package_ndc": "76420-030-30", "marketing_start_date": "20200619"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-030-60)", "package_ndc": "76420-030-60", "marketing_start_date": "20200619"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-030-90)", "package_ndc": "76420-030-90", "marketing_start_date": "20200619"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "76420-030_e4ec0115-3fdf-8c05-e053-2995a90a8353", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-030", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}