Package 70518-1765-1

{"route": ["ORAL"], "spl_id": "49741c96-db6d-402a-e063-6394a90a07e4", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596930"], "spl_set_id": ["1d3a45f3-3854-4d0c-9241-770aa24063fd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1765-1)", "package_ndc": "70518-1765-1", "marketing_start_date": "20250122"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1765-2)", "package_ndc": "70518-1765-2", "marketing_start_date": "20250623"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1765-3)", "package_ndc": "70518-1765-3", "marketing_start_date": "20250808"}], "brand_name": "Duloxetine", "product_id": "70518-1765_49741c96-db6d-402a-e063-6394a90a07e4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1765", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20190102", "listing_expiration_date": "20271231"}