Package 50090-6854-0

{"route": ["ORAL"], "spl_id": "38b796d8-75a7-4fef-9e33-0adaca3de95e", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["0e1d17d5-d39c-4144-aac0-7c0d3bc9ec0d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6854-0)", "package_ndc": "50090-6854-0", "marketing_start_date": "20231130"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6854-1)", "package_ndc": "50090-6854-1", "marketing_start_date": "20231130"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6854-2)", "package_ndc": "50090-6854-2", "marketing_start_date": "20231130"}], "brand_name": "Gabapentin", "product_id": "50090-6854_38b796d8-75a7-4fef-9e33-0adaca3de95e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-6854", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20271231"}