Package 67877-265-30

{"route": ["ORAL"], "spl_id": "958fae45-5e7a-4f8b-80b7-5934222747b5", "openfda": {"upc": ["0367877263106"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["e6477c41-97a2-45a7-94b5-487aa65199f6"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-01)", "package_ndc": "67877-265-01", "marketing_start_date": "20120501"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-10)", "package_ndc": "67877-265-10", "marketing_start_date": "20120501"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-30)", "package_ndc": "67877-265-30", "marketing_start_date": "20120501"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-90)", "package_ndc": "67877-265-90", "marketing_start_date": "20120501"}], "brand_name": "Duloxetine", "product_id": "67877-265_958fae45-5e7a-4f8b-80b7-5934222747b5", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "67877-265", "generic_name": "Duloxetine", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA203197", "marketing_category": "ANDA", "marketing_start_date": "20120501", "listing_expiration_date": "20261231"}