Package 68071-2375-9
Brand: fluoxetine
Generic: fluoxetine hydrochloridePackage Facts
Identity
Package NDC
68071-2375-9
Digits Only
6807123759
Product NDC
68071-2375
Description
90 CAPSULE in 1 BOTTLE (68071-2375-9)
Marketing
Marketing Status
Brand
fluoxetine
Generic
fluoxetine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29a539bb-42ee-dc73-e063-6394a90a5fe9", "openfda": {"upc": ["0368071237535"], "unii": ["I9W7N6B1KJ"], "rxcui": ["313989"], "spl_set_id": ["be4c5102-e0aa-3b89-e053-2a95a90a5d9d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-2375-3)", "package_ndc": "68071-2375-3", "marketing_start_date": "20210324"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68071-2375-9)", "package_ndc": "68071-2375-9", "marketing_start_date": "20241219"}], "brand_name": "Fluoxetine", "product_id": "68071-2375_29a539bb-42ee-dc73-e063-6394a90a5fe9", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-2375", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20150316", "listing_expiration_date": "20261231"}