Package 60687-518-01

{"route": ["ORAL"], "spl_id": "37dcca50-b1a8-24e7-e063-6394a90a8adf", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["765c7ce0-bbf5-4265-8ff0-1ba092c69865"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-518-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-518-11)", "package_ndc": "60687-518-01", "marketing_start_date": "20200302"}], "brand_name": "Gabapentin", "product_id": "60687-518_37dcca50-b1a8-24e7-e063-6394a90a8adf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60687-518", "generic_name": "Gabapentin", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA078926", "marketing_category": "ANDA", "marketing_start_date": "20200302", "listing_expiration_date": "20261231"}