Package 71205-005-60

{"route": ["ORAL"], "spl_id": "9897ad4f-87a5-40c8-8c79-7638eae42437", "openfda": {"upc": ["0371205005603"], "unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["5410084d-a7db-4da1-a45d-24b91ef50404"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-30)", "package_ndc": "71205-005-30", "marketing_start_date": "20180402"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-60)", "package_ndc": "71205-005-60", "marketing_start_date": "20180402"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-90)", "package_ndc": "71205-005-90", "marketing_start_date": "20180402"}], "brand_name": "Duloxetine", "product_id": "71205-005_9897ad4f-87a5-40c8-8c79-7638eae42437", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-005", "generic_name": "Duloxetine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20170316", "listing_expiration_date": "20261231"}