Package 62332-647-31

{"route": ["ORAL"], "spl_id": "56acaace-062b-48f0-a75d-db44bf35120d", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["3cdde96c-9fc9-4698-872a-25c05318ecb5"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-647-31)", "package_ndc": "62332-647-31", "marketing_start_date": "20100218"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-647-71)", "package_ndc": "62332-647-71", "marketing_start_date": "20100218"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-647-91)", "package_ndc": "62332-647-91", "marketing_start_date": "20100218"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "62332-647_56acaace-062b-48f0-a75d-db44bf35120d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "62332-647", "generic_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078218", "marketing_category": "ANDA", "marketing_start_date": "20100218", "listing_expiration_date": "20261231"}