Package 51655-539-52

{"route": ["ORAL"], "spl_id": "494dea9c-f9af-2eec-e063-6294a90ab96f", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["dae3be94-a40c-5be1-e053-2a95a90a1484"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-20)", "package_ndc": "51655-539-20", "marketing_start_date": "20210114"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-52)", "package_ndc": "51655-539-52", "marketing_start_date": "20210526"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-539-53)", "package_ndc": "51655-539-53", "marketing_start_date": "20220415"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "51655-539_494dea9c-f9af-2eec-e063-6294a90ab96f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "51655-539", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20210114", "listing_expiration_date": "20271231"}