Package 63629-5930-1

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 63629-5930-1
Digits Only 6362959301
Product NDC 63629-5930
Product ID 63629-5930_4b756a64-ce57-4db2-b70f-681d542a1133
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-5930-1)

Marketing

Marketing Status
Marketed Since 2025-06-02
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": "4b756a64-ce57-4db2-b70f-681d542a1133", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313990"], "spl_set_id": ["ada19ae4-f3bd-47fa-a5c3-a6bb3aa34943"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-5930-1)", "package_ndc": "63629-5930-1", "marketing_start_date": "20250602"}], "brand_name": "Fluoxetine", "product_id": "63629-5930_4b756a64-ce57-4db2-b70f-681d542a1133", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-5930", "generic_name": "Fluoxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208698", "marketing_category": "ANDA", "marketing_start_date": "20170407", "listing_expiration_date": "20261231"}