Package 80425-0087-1

{"route": ["ORAL"], "spl_id": "2a98ff70-0368-7169-e063-6394a90adc74", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["b2db3979-daa6-6e83-e053-2a95a90a3a2f"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0087-1)", "package_ndc": "80425-0087-1", "marketing_start_date": "20070504"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0087-2)", "package_ndc": "80425-0087-2", "marketing_start_date": "20070504"}], "brand_name": "Zolpidem Tartrate", "product_id": "80425-0087_2a98ff70-0368-7169-e063-6394a90adc74", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "80425-0087", "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": "ANDA078413", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20261231"}