Package 68788-8854-3

{"route": ["ORAL"], "spl_id": "d579c6ca-c820-49ff-92fb-2e6aaad3b052", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["d579c6ca-c820-49ff-92fb-2e6aaad3b052"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-8854-3)", "package_ndc": "68788-8854-3", "marketing_start_date": "20250411"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-8854-6)", "package_ndc": "68788-8854-6", "marketing_start_date": "20250411"}], "brand_name": "Zolpidem Tartrate", "product_id": "68788-8854_d579c6ca-c820-49ff-92fb-2e6aaad3b052", "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": "68788-8854", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20250411", "listing_expiration_date": "20261231"}