Package 76420-636-20

{"route": ["ORAL"], "spl_id": "31e2603c-b629-1f0d-e063-6294a90a3646", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["f61bd9f3-cd3d-4c76-a110-0f1dcba610af"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-01)", "package_ndc": "76420-636-01", "marketing_start_date": "20231017"}, {"sample": false, "description": "20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-20)", "package_ndc": "76420-636-20", "marketing_start_date": "20250403"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-30)", "package_ndc": "76420-636-30", "marketing_start_date": "20231017"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-90)", "package_ndc": "76420-636-90", "marketing_start_date": "20231017"}], "brand_name": "Duloxetine", "product_id": "76420-636_31e2603c-b629-1f0d-e063-6294a90a3646", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "76420-636", "generic_name": "Duloxetine", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208706", "marketing_category": "ANDA", "marketing_start_date": "20190325", "listing_expiration_date": "20261231"}