Package 46708-243-91

{"route": ["ORAL"], "spl_id": "563f5910-59e7-46c6-9b3d-d9c9b0efb350", "openfda": {"upc": ["0346708242305"], "unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["9c5112c0-c721-4086-9a75-3b7f931430bb"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-243-30)", "package_ndc": "46708-243-30", "marketing_start_date": "20170415"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-243-31)", "package_ndc": "46708-243-31", "marketing_start_date": "20170415"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-243-91)", "package_ndc": "46708-243-91", "marketing_start_date": "20170415"}], "brand_name": "Fluoxetine Hydrochloride", "product_id": "46708-243_563f5910-59e7-46c6-9b3d-d9c9b0efb350", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "46708-243", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine Hydrochloride", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208698", "marketing_category": "ANDA", "marketing_start_date": "20170415", "listing_expiration_date": "20261231"}