Package 77771-177-90

{"route": ["ORAL"], "spl_id": "2b2895a0-b3d1-4aa0-ac06-3b6983bdcd2d", "openfda": {"nui": ["N0000008486"], "upc": ["0377771178901", "0377771177904", "0377771178055"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["1045db4e-4c76-4a0d-bf12-019bd96a8f59"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Radha Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (77771-177-05)", "package_ndc": "77771-177-05", "marketing_start_date": "20231103"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (77771-177-90)", "package_ndc": "77771-177-90", "marketing_start_date": "20231103"}], "brand_name": "Gabapentin", "product_id": "77771-177_2b2895a0-b3d1-4aa0-ac06-3b6983bdcd2d", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "77771-177", "generic_name": "Gabapentin", "labeler_name": "Radha Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20231103", "listing_expiration_date": "20261231"}