Package 71610-736-42

{"route": ["ORAL"], "spl_id": "0c2b6f3c-0c28-4eff-be0d-cf22961050a3", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["dcfd62c7-1687-4e9b-9ae4-5a44929ac765"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1800 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-736-42)", "package_ndc": "71610-736-42", "marketing_start_date": "20230915"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "71610-736_0c2b6f3c-0c28-4eff-be0d-cf22961050a3", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-736", "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"}