Package 63629-2201-1

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 63629-2201-1
Digits Only 6362922011
Product NDC 63629-2201
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-2201-1)

Marketing

Marketing Status
Marketed Since 2022-10-28
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": "ff509ee8-400d-4128-aab8-5b389dd7f082", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["10293946-5a06-4c21-9f78-941be360b09b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-2201-1)", "package_ndc": "63629-2201-1", "marketing_start_date": "20221028"}], "brand_name": "Fluoxetine", "product_id": "63629-2201_ff509ee8-400d-4128-aab8-5b389dd7f082", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-2201", "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"}