Package 68180-294-03

{"route": ["ORAL"], "spl_id": "7efa28f3-0b15-4e1c-835f-2f1dff37bee8", "openfda": {"unii": ["9044SC542W"], "rxcui": ["596926", "596930", "596934", "616402"], "spl_set_id": ["829a4f51-c882-4b64-81f3-abfb03a52ebe"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-03)", "package_ndc": "68180-294-03", "marketing_start_date": "20131211"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-07)", "package_ndc": "68180-294-07", "marketing_start_date": "20131211"}], "brand_name": "Duloxetine", "product_id": "68180-294_7efa28f3-0b15-4e1c-835f-2f1dff37bee8", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68180-294", "generic_name": "Duloxetine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duloxetine", "active_ingredients": [{"name": "DULOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA090694", "marketing_category": "ANDA", "marketing_start_date": "20131211", "listing_expiration_date": "20261231"}