Package 50090-6189-0

{"route": ["ORAL"], "spl_id": "293a0007-ee4b-46b0-a69e-2ff3622ddcf3", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["40bb60c0-a2f3-4e7f-b13c-028c906c4852"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6189-0)", "package_ndc": "50090-6189-0", "marketing_start_date": "20221027"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6189-1)", "package_ndc": "50090-6189-1", "marketing_start_date": "20221027"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6189-2)", "package_ndc": "50090-6189-2", "marketing_start_date": "20221027"}], "brand_name": "GABAPENTIN", "product_id": "50090-6189_293a0007-ee4b-46b0-a69e-2ff3622ddcf3", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-6189", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA214957", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}