Package 72189-178-90

{"route": ["ORAL"], "spl_id": "2becf606-de3d-b686-e063-6294a90afe58", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310432", "310434"], "spl_set_id": ["a7e45e3f-e382-32ba-e053-2a95a90a2537"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-178-30)", "package_ndc": "72189-178-30", "marketing_start_date": "20210208"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-178-72)", "package_ndc": "72189-178-72", "marketing_start_date": "20210208"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-178-90)", "package_ndc": "72189-178-90", "marketing_start_date": "20210208"}], "brand_name": "GABAPENTIN", "product_id": "72189-178_2becf606-de3d-b686-e063-6294a90afe58", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-178", "generic_name": "GABAPENTIN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20210208", "listing_expiration_date": "20261231"}