Package 72789-127-90

{"route": ["ORAL"], "spl_id": "4af71629-cd0b-2e7c-e063-6394a90a2eab", "openfda": {"nui": ["N0000008486"], "upc": ["0372789127903"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["81774da8-cb1d-4c7d-8550-35396850d5ff"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-127-30)", "package_ndc": "72789-127-30", "marketing_start_date": "20200925"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-127-90)", "package_ndc": "72789-127-90", "marketing_start_date": "20221201"}], "brand_name": "Gabapentin", "product_id": "72789-127_4af71629-cd0b-2e7c-e063-6394a90a2eab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72789-127", "generic_name": "Gabapentin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA078926", "marketing_category": "ANDA", "marketing_start_date": "20121016", "listing_expiration_date": "20271231"}