Package 50111-647-01

{"route": ["ORAL"], "spl_id": "424ed364-e023-472f-b113-673e9342a7f1", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384", "310385"], "spl_set_id": ["06d71a33-5578-4012-b11d-764f45bc1e6a"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50111-647-01)", "package_ndc": "50111-647-01", "marketing_start_date": "20020129"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (50111-647-02)", "package_ndc": "50111-647-02", "marketing_start_date": "20020129"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (50111-647-03)", "package_ndc": "50111-647-03", "marketing_start_date": "20020129"}], "brand_name": "Fluoxetine", "product_id": "50111-647_424ed364-e023-472f-b113-673e9342a7f1", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50111-647", "generic_name": "Fluoxetine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076001", "marketing_category": "ANDA", "marketing_start_date": "20020129", "listing_expiration_date": "20261231"}