Package 50228-638-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50228-638-30
Digits Only 5022863830
Product NDC 50228-638
Description

30 TABLET in 1 BOTTLE (50228-638-30)

Marketing

Marketing Status
Marketed Since 2025-09-11
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e89095f-77b2-4fde-e063-6294a90a1ff3", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["3e8912e2-2a0c-5047-e063-6294a90a7e32"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-638-10)", "package_ndc": "50228-638-10", "marketing_start_date": "20250911"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-638-30)", "package_ndc": "50228-638-30", "marketing_start_date": "20250911"}], "brand_name": "Fluoxetine", "product_id": "50228-638_3e89095f-77b2-4fde-e063-6294a90a1ff3", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50228-638", "generic_name": "FLUOXETINE HYDROCHLORIDE", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211282", "marketing_category": "ANDA", "marketing_start_date": "20250911", "listing_expiration_date": "20261231"}