Package 72162-1600-3

{"route": ["ORAL"], "spl_id": "075f61b7-af66-42ee-8275-c9d9f01fc074", "openfda": {"unii": ["9044SC542W"], "rxcui": ["616402"], "spl_set_id": ["f66f63c8-51db-4183-a452-78205cf3a263"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1600-3)", "package_ndc": "72162-1600-3", "marketing_start_date": "20180521"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "72162-1600_075f61b7-af66-42ee-8275-c9d9f01fc074", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72162-1600", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "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"}