Package 43063-611-90

{"route": ["ORAL"], "spl_id": "2cda4edb-3ee5-0035-e063-6294a90a7800", "openfda": {"nui": ["N0000008486"], "upc": ["0343063611609"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["d22ed424-f365-44ca-8ef9-a08255a90ae8"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-611-60)", "package_ndc": "43063-611-60", "marketing_start_date": "20250129"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-611-90)", "package_ndc": "43063-611-90", "marketing_start_date": "20150504"}], "brand_name": "Gabapentin", "product_id": "43063-611_2cda4edb-3ee5-0035-e063-6294a90a7800", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "43063-611", "generic_name": "Gabapentin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20121016", "listing_expiration_date": "20261231"}