Package 51991-747-33

{"route": ["ORAL"], "spl_id": "32327581-bdab-41ac-9adc-bf208e1c4e42", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["caef6f50-1571-4ec7-8f8c-42b924d323ee"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10)", "package_ndc": "51991-747-10", "marketing_start_date": "20140611"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-33)", "package_ndc": "51991-747-33", "marketing_start_date": "20140611"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-90)", "package_ndc": "51991-747-90", "marketing_start_date": "20140611"}], "brand_name": "Duloxetine Delayed-Release", "product_id": "51991-747_32327581-bdab-41ac-9adc-bf208e1c4e42", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51991-747", "generic_name": "DULOXETINE HYDROCHLORIDE", "labeler_name": "Breckenridge Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "brand_name_suffix": "Delayed-Release", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203088", "marketing_category": "ANDA", "marketing_start_date": "20140611", "listing_expiration_date": "20261231"}