Package 59651-324-30

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 59651-324-30
Digits Only 5965132430
Product NDC 59651-324
Product ID 59651-324_5f402504-f531-4cbf-95d5-fe23b90630b2
Description

30 TABLET, FILM COATED in 1 BOTTLE (59651-324-30)

Marketing

Marketing Status
Marketed Since 2020-06-10
Brand fluoxetine
Generic fluoxetine
Sample Package No

Linked Drug Pages (1)

Fluoxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5f402504-f531-4cbf-95d5-fe23b90630b2", "openfda": {"upc": ["0359651324301"], "unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["5336ce59-7a6c-4db9-8512-299cc5e599c0"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59651-324-30)", "package_ndc": "59651-324-30", "marketing_start_date": "20200610"}], "brand_name": "Fluoxetine", "product_id": "59651-324_5f402504-f531-4cbf-95d5-fe23b90630b2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "59651-324", "generic_name": "Fluoxetine", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA213265", "marketing_category": "ANDA", "marketing_start_date": "20200610", "listing_expiration_date": "20261231"}