Package 47335-383-61

{"route": ["ORAL"], "spl_id": "cec0154d-5c8c-496d-89bd-ba2a93aee774", "openfda": {"upc": ["0347335383836", "0347335382839"], "unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934"], "spl_set_id": ["f16beb64-5878-486a-82ee-8e83e728f26c"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-08)", "package_ndc": "47335-383-08", "marketing_start_date": "20131211"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-18)", "package_ndc": "47335-383-18", "marketing_start_date": "20131211"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (47335-383-61)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "47335-383-61", "marketing_start_date": "20131211"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-83)", "package_ndc": "47335-383-83", "marketing_start_date": "20131211"}, {"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-383-88)", "package_ndc": "47335-383-88", "marketing_start_date": "20131211"}], "brand_name": "Duloxetine", "product_id": "47335-383_cec0154d-5c8c-496d-89bd-ba2a93aee774", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "47335-383", "generic_name": "Duloxetine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA090745", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}