Package 71610-218-60

{"route": ["ORAL"], "spl_id": "492c2d4f-3ba2-4858-bfbb-8ade6b3b7e30", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["db686a0a-9b2a-4017-8bd1-b981da47c2f3"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-218-30)", "package_ndc": "71610-218-30", "marketing_start_date": "20190107"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-218-60)", "package_ndc": "71610-218-60", "marketing_start_date": "20190107"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "71610-218_492c2d4f-3ba2-4858-bfbb-8ade6b3b7e30", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71610-218", "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"}