Package 53746-541-01

{"route": ["ORAL"], "spl_id": "b0e32570-da9f-4fa8-a0a2-0334fce7ff7a", "openfda": {"upc": ["0353746540010", "0353746541017"], "unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["31bb92f6-ec8c-4636-8b07-8814417fe78e"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (53746-541-01)", "package_ndc": "53746-541-01", "marketing_start_date": "20100218"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (53746-541-05)", "package_ndc": "53746-541-05", "marketing_start_date": "20100218"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (53746-541-10)", "package_ndc": "53746-541-10", "marketing_start_date": "20100218"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "53746-541_b0e32570-da9f-4fa8-a0a2-0334fce7ff7a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "53746-541", "generic_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078218", "marketing_category": "ANDA", "marketing_start_date": "20100218", "listing_expiration_date": "20261231"}