Package 68788-8688-3

{"route": ["ORAL"], "spl_id": "c5b2bddf-74f7-48c8-b6ab-1cfc05dab3f5", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["156fe804-d674-4b52-82f5-6cd7715c707b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8688-1)", "package_ndc": "68788-8688-1", "marketing_start_date": "20240605"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8688-3)", "package_ndc": "68788-8688-3", "marketing_start_date": "20240605"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8688-6)", "package_ndc": "68788-8688-6", "marketing_start_date": "20240605"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-8688-8)", "package_ndc": "68788-8688-8", "marketing_start_date": "20240605"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8688-9)", "package_ndc": "68788-8688-9", "marketing_start_date": "20240605"}], "brand_name": "Gabapentin", "product_id": "68788-8688_c5b2bddf-74f7-48c8-b6ab-1cfc05dab3f5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68788-8688", "generic_name": "GABAPENTIN", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20240605", "listing_expiration_date": "20261231"}