Package 43353-960-83

{"route": ["ORAL"], "spl_id": "159efe2d-21ab-358f-e063-6394a90a8ded", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["c94339ab-3aaf-4cc9-b770-650b433bcce8"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (43353-960-30)", "package_ndc": "43353-960-30", "marketing_start_date": "20170809"}, {"sample": false, "description": "1800 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (43353-960-42)", "package_ndc": "43353-960-42", "marketing_start_date": "20230217"}, {"sample": false, "description": "3600 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (43353-960-83)", "package_ndc": "43353-960-83", "marketing_start_date": "20140814"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "43353-960_159efe2d-21ab-358f-e063-6394a90a8ded", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43353-960", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}