Package 68788-8362-0

{"route": ["ORAL"], "spl_id": "19b034a2-26d7-4c9b-b8a6-391e06a31adb", "openfda": {"unii": ["9044SC542W"], "rxcui": ["616402"], "spl_set_id": ["2c233b3f-83de-40c4-9f1d-81f901f89459"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-0)", "package_ndc": "68788-8362-0", "marketing_start_date": "20230314"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)", "package_ndc": "68788-8362-3", "marketing_start_date": "20230201"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-9)", "package_ndc": "68788-8362-9", "marketing_start_date": "20230201"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "68788-8362_19b034a2-26d7-4c9b-b8a6-391e06a31adb", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8362", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20230201", "listing_expiration_date": "20261231"}