Package 68094-489-60

{"route": ["ORAL"], "spl_id": "471ad25b-0c63-489c-9df3-44ea7fdcd256", "openfda": {"nui": ["N0000008486"], "upc": ["0368094589505"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["86c93d8b-6286-44e2-93dd-f1b10a5d83da"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Precision Dose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (68094-489-50)", "package_ndc": "68094-489-50", "marketing_start_date": "20240215"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (68094-489-60)", "package_ndc": "68094-489-60", "marketing_start_date": "20240215"}], "brand_name": "Gabapentin", "product_id": "68094-489_471ad25b-0c63-489c-9df3-44ea7fdcd256", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68094-489", "generic_name": "Gabapentin", "labeler_name": "Precision Dose, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}