Package 71610-743-53

{"route": ["ORAL"], "spl_id": "3724601a-53f8-5bd3-e063-6394a90a98a6", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596934"], "spl_set_id": ["3bae1317-4cc8-4d86-b1b6-15edee733a6d"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-30)", "package_ndc": "71610-743-30", "marketing_start_date": "20231016"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-53)", "package_ndc": "71610-743-53", "marketing_start_date": "20231016"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-60)", "package_ndc": "71610-743-60", "marketing_start_date": "20231016"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-74)", "package_ndc": "71610-743-74", "marketing_start_date": "20250605"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-80)", "package_ndc": "71610-743-80", "marketing_start_date": "20240320"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "71610-743_3724601a-53f8-5bd3-e063-6394a90a98a6", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-743", "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": "60 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}