Package 80425-0513-1

{"route": ["ORAL"], "spl_id": "3310d645-9b5f-16f5-e063-6294a90a9eb5", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["3310d63e-d79a-175d-e063-6394a90a4270"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (80425-0513-1)", "package_ndc": "80425-0513-1", "marketing_start_date": "20250415"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (80425-0513-2)", "package_ndc": "80425-0513-2", "marketing_start_date": "20250415"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (80425-0513-3)", "package_ndc": "80425-0513-3", "marketing_start_date": "20250415"}], "brand_name": "Zolpidem Tartrate", "product_id": "80425-0513_3310d645-9b5f-16f5-e063-6294a90a9eb5", "dosage_form": "TABLET, COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "80425-0513", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA077322", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}