Package 72162-1506-3

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 72162-1506-3
Digits Only 7216215063
Product NDC 72162-1506
Product ID 72162-1506_cf0b39d7-583f-43cc-9737-e28c00ff392c
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-1506-3)

Marketing

Marketing Status
Marketed Since 2024-04-08
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": "cf0b39d7-583f-43cc-9737-e28c00ff392c", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["dced86a0-fc08-465c-897c-f8899e6206d5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1506-3)", "package_ndc": "72162-1506-3", "marketing_start_date": "20240408"}], "brand_name": "Fluoxetine", "product_id": "72162-1506_cf0b39d7-583f-43cc-9737-e28c00ff392c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-1506", "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": "ANDA209419", "marketing_category": "ANDA", "marketing_start_date": "20171116", "listing_expiration_date": "20261231"}