Package 51655-427-53

{"route": ["ORAL"], "spl_id": "490ec87f-5dd5-d491-e063-6294a90aff60", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["c29cf8bd-2f63-ed4b-e053-2995a90ab6eb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-26)", "package_ndc": "51655-427-26", "marketing_start_date": "20210401"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-52)", "package_ndc": "51655-427-52", "marketing_start_date": "20220413"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-427-53)", "package_ndc": "51655-427-53", "marketing_start_date": "20200901"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "51655-427_490ec87f-5dd5-d491-e063-6294a90aff60", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "51655-427", "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": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20200901", "listing_expiration_date": "20271231"}