Package 70518-1139-4

{"route": ["ORAL"], "spl_id": "485b3c93-6f32-6ee9-e063-6294a90a13a7", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926"], "spl_set_id": ["9286ec0b-45ae-4a09-a0ad-556ec92aab63"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-0)", "package_ndc": "70518-1139-0", "marketing_start_date": "20180425"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1139-1)", "package_ndc": "70518-1139-1", "marketing_start_date": "20250109"}, {"sample": false, "description": "180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1139-2)", "package_ndc": "70518-1139-2", "marketing_start_date": "20250416"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1139-3)", "package_ndc": "70518-1139-3", "marketing_start_date": "20250613"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-4)", "package_ndc": "70518-1139-4", "marketing_start_date": "20251227"}], "brand_name": "Duloxetine", "product_id": "70518-1139_485b3c93-6f32-6ee9-e063-6294a90a13a7", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1139", "generic_name": "Duloxetine", "labeler_name": "REMEDYREPACK INC.", "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": "20180425", "listing_expiration_date": "20271231"}