Package 71610-403-53

{"route": ["ORAL"], "spl_id": "43cd971a-bb4a-b6ca-e063-6394a90af045", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["c482d64a-73dd-4af2-9b3c-efff47e7395c"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-403-53)", "package_ndc": "71610-403-53", "marketing_start_date": "20251114"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-403-60)", "package_ndc": "71610-403-60", "marketing_start_date": "20200309"}], "brand_name": "Duloxetine", "product_id": "71610-403_43cd971a-bb4a-b6ca-e063-6394a90af045", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-403", "generic_name": "Duloxetine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}