Package 71335-2597-1

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 71335-2597-1
Digits Only 7133525971
Product NDC 71335-2597
Product ID 71335-2597_40272603-bcda-461e-b7a8-dcce9398c268
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2597-1)

Marketing

Marketing Status
Marketed Since 2025-02-12
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": "40272603-bcda-461e-b7a8-dcce9398c268", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["7a631271-9597-42a4-a924-1d06ecaba8c8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2597-1)", "package_ndc": "71335-2597-1", "marketing_start_date": "20250212"}], "brand_name": "Fluoxetine", "product_id": "71335-2597_40272603-bcda-461e-b7a8-dcce9398c268", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-2597", "generic_name": "Fluoxetine", "labeler_name": "Bryant Ranch Prepack", "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"}