Package 62332-243-30

{"route": ["ORAL"], "spl_id": "80f85fbd-5e1b-424d-b017-e3caa30131bb", "openfda": {"upc": ["0362332243303", "0362332242306"], "unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["e9ee6e93-4a57-4fd1-a417-3944484dd32c"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-243-30)", "package_ndc": "62332-243-30", "marketing_start_date": "20170407"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-243-31)", "package_ndc": "62332-243-31", "marketing_start_date": "20170407"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-243-91)", "package_ndc": "62332-243-91", "marketing_start_date": "20170407"}], "brand_name": "Fluoxetine", "product_id": "62332-243_80f85fbd-5e1b-424d-b017-e3caa30131bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "62332-243", "generic_name": "Fluoxetine", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208698", "marketing_category": "ANDA", "marketing_start_date": "20170407", "listing_expiration_date": "20261231"}