Package 64380-903-06

{"route": ["ORAL"], "spl_id": "35d9874e-1471-484c-b625-29e70a190e10", "openfda": {"upc": ["0364380902065", "0364380903062"], "unii": ["I9W7N6B1KJ"], "rxcui": ["248642", "313990"], "spl_set_id": ["ca749349-d0e1-4b7c-b4c0-e392e72cf0f6"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (64380-903-04)", "package_ndc": "64380-903-04", "marketing_start_date": "20240812"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (64380-903-06)", "package_ndc": "64380-903-06", "marketing_start_date": "20240812"}], "brand_name": "FLUOXETINE", "product_id": "64380-903_35d9874e-1471-484c-b625-29e70a190e10", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "64380-903", "generic_name": "fluoxetine", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUOXETINE", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA212684", "marketing_category": "ANDA", "marketing_start_date": "20240812", "listing_expiration_date": "20271231"}