Package 72162-1597-9

{"route": ["ORAL"], "spl_id": "9f31e892-c621-4a83-98a3-41e2fcd53f8e", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["a5804a0b-ceae-4ebd-bba0-bfc10e21b90d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1597-5)", "package_ndc": "72162-1597-5", "marketing_start_date": "20240205"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1597-9)", "package_ndc": "72162-1597-9", "marketing_start_date": "20240205"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "72162-1597_9f31e892-c621-4a83-98a3-41e2fcd53f8e", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72162-1597", "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": "20 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}