Package 82804-024-30

{"route": ["ORAL"], "spl_id": "f5e7503a-b28f-4cd0-a4ee-47bdca88d54b", "openfda": {"upc": ["0382804024308"], "unii": ["9044SC542W"], "rxcui": ["616402"], "spl_set_id": ["f5e7503a-b28f-4cd0-a4ee-47bdca88d54b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-30)", "package_ndc": "82804-024-30", "marketing_start_date": "20231016"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60)", "package_ndc": "82804-024-60", "marketing_start_date": "20231016"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90)", "package_ndc": "82804-024-90", "marketing_start_date": "20231016"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "82804-024_f5e7503a-b28f-4cd0-a4ee-47bdca88d54b", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82804-024", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20180521", "listing_expiration_date": "20261231"}