Package 10702-007-09

{"route": ["ORAL"], "spl_id": "7d541fa9-d74b-5236-e053-2991aa0acc0e", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["5b756c04-e7b8-4efe-815a-3f3e020727fb"], "manufacturer_name": ["KVK-TECH, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10702-007-01)", "package_ndc": "10702-007-01", "marketing_start_date": "20140731"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (10702-007-03)", "package_ndc": "10702-007-03", "marketing_start_date": "20140731"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (10702-007-09)", "package_ndc": "10702-007-09", "marketing_start_date": "20181129"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (10702-007-10)", "package_ndc": "10702-007-10", "marketing_start_date": "20140731"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (10702-007-50)", "package_ndc": "10702-007-50", "marketing_start_date": "20140731"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "10702-007_7d541fa9-d74b-5236-e053-2991aa0acc0e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "10702-007", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "KVK-TECH, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078048", "marketing_category": "ANDA", "marketing_start_date": "20140731", "listing_expiration_date": "20261231"}