Package 68071-2659-6

{"route": ["ORAL"], "spl_id": "2a2f9ff7-41b4-0f91-e063-6294a90af9b6", "openfda": {"upc": ["0368071265934"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["db49801d-9bde-5dd0-e053-2a95a90aee53"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3)", "package_ndc": "68071-2659-3", "marketing_start_date": "20220328"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5)", "package_ndc": "68071-2659-5", "marketing_start_date": "20220328"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6)", "package_ndc": "68071-2659-6", "marketing_start_date": "20241014"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7)", "package_ndc": "68071-2659-7", "marketing_start_date": "20241202"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68071-2659_2a2f9ff7-41b4-0f91-e063-6294a90af9b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-2659", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}