Package 68382-356-01

{"route": ["ORAL"], "spl_id": "898c1710-d86c-4fbe-9a53-34661fcdb63a", "openfda": {"nui": ["N0000008486"], "upc": ["0368382607164"], "unii": ["6CW7F3G59X"], "rxcui": ["1806380", "1806382", "2634743", "2634747", "2634751"], "spl_set_id": ["3cfd04ab-e421-441f-a10e-e4dd1412974d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-356-01)", "package_ndc": "68382-356-01", "marketing_start_date": "20250918"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68382-356-14)", "package_ndc": "68382-356-14", "marketing_start_date": "20250918"}], "brand_name": "gabapentin", "product_id": "68382-356_898c1710-d86c-4fbe-9a53-34661fcdb63a", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68382-356", "generic_name": "gabapentin", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "750 mg/1"}], "application_number": "ANDA203934", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}