Package 76420-651-90

{"route": ["ORAL"], "spl_id": "0e42e402-85e4-30a1-e063-6394a90a142c", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["433798", "433799", "433800", "433801"], "spl_set_id": ["5d839a8b-0f45-42bf-acc1-2bd28f948e53"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-651-30)", "package_ndc": "76420-651-30", "marketing_start_date": "20240105"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-651-60)", "package_ndc": "76420-651-60", "marketing_start_date": "20240105"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-651-90)", "package_ndc": "76420-651-90", "marketing_start_date": "20240105"}], "brand_name": "Alprazolam", "product_id": "76420-651_0e42e402-85e4-30a1-e063-6394a90a142c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "76420-651", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "ANDA090871", "marketing_category": "ANDA", "marketing_start_date": "20110607", "listing_expiration_date": "20261231"}