Package 71205-445-30

{"route": ["ORAL"], "spl_id": "d0a48dfd-af34-470b-9e1f-7678203e9ae5", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["d0a48dfd-af34-470b-9e1f-7678203e9ae5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-30)", "package_ndc": "71205-445-30", "marketing_start_date": "20200519"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-60)", "package_ndc": "71205-445-60", "marketing_start_date": "20200519"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-90)", "package_ndc": "71205-445-90", "marketing_start_date": "20200519"}], "brand_name": "Duloxetine", "product_id": "71205-445_d0a48dfd-af34-470b-9e1f-7678203e9ae5", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71205-445", "generic_name": "Duloxetine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203197", "marketing_category": "ANDA", "marketing_start_date": "20120501", "listing_expiration_date": "20261231"}