Package 68462-126-05

{"route": ["ORAL"], "spl_id": "4da1bae0-701b-4b65-a01e-f4bcedfad849", "openfda": {"nui": ["N0000008486"], "upc": ["0368462127018", "0368462126011"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["3865a6e3-112c-490c-82ac-35401336b16e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68462-126-01)", "package_ndc": "68462-126-01", "marketing_start_date": "20060401"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68462-126-05)", "package_ndc": "68462-126-05", "marketing_start_date": "20060401"}], "brand_name": "Gabapentin", "product_id": "68462-126_4da1bae0-701b-4b65-a01e-f4bcedfad849", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68462-126", "generic_name": "Gabapentin", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA077662", "marketing_category": "ANDA", "marketing_start_date": "20060401", "listing_expiration_date": "20261231"}