Package 68999-730-24
Brand: fluoxetine
Generic: fluoxetinePackage Facts
Identity
Package NDC
68999-730-24
Digits Only
6899973024
Product NDC
68999-730
Description
2 TRAY in 1 BOX (68999-730-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-730-45)
Marketing
Marketing Status
Brand
fluoxetine
Generic
fluoxetine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a935e59-bd47-9aae-e063-6394a90aad58", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["d34362ed-e821-4c55-9f8c-3dfb772b1b2a"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-730-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-730-45)", "package_ndc": "68999-730-24", "marketing_start_date": "20251031"}], "brand_name": "Fluoxetine", "product_id": "68999-730_4a935e59-bd47-9aae-e063-6394a90aad58", "dosage_form": "LIQUID", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68999-730", "generic_name": "Fluoxetine", "labeler_name": "Chartwell Governmental & Specialty RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA076458", "marketing_category": "ANDA", "marketing_start_date": "20040514", "listing_expiration_date": "20271231"}