Package 51655-592-52

{"route": ["ORAL"], "spl_id": "49612fd2-0c18-42a0-e063-6394a90a00fc", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["f32bceda-1d24-322d-e053-2995a90aae1b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-20)", "package_ndc": "51655-592-20", "marketing_start_date": "20230131"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-25)", "package_ndc": "51655-592-25", "marketing_start_date": "20230502"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-26)", "package_ndc": "51655-592-26", "marketing_start_date": "20230207"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-52)", "package_ndc": "51655-592-52", "marketing_start_date": "20230103"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-53)", "package_ndc": "51655-592-53", "marketing_start_date": "20230103"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-592-54)", "package_ndc": "51655-592-54", "marketing_start_date": "20230103"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "51655-592_49612fd2-0c18-42a0-e063-6394a90a00fc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "51655-592", "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": "20230103", "listing_expiration_date": "20271231"}