Package 50228-422-30

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50228-422-30
Digits Only 5022842230
Product NDC 50228-422
Product ID 50228-422_2c27d964-db05-c709-e063-6294a90a385c
Description

30 TABLET in 1 BOTTLE (50228-422-30)

Marketing

Marketing Status
Marketed Since 2019-01-10
Brand fluoxetine
Generic fluoxetine hydrochloride
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": "2c27d964-db05-c709-e063-6294a90a385c", "openfda": {"upc": ["0350228422307"], "unii": ["I9W7N6B1KJ"], "rxcui": ["1190110"], "spl_set_id": ["a7ba9184-7dad-4f82-a947-bb2cc6b760ce"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-422-10)", "package_ndc": "50228-422-10", "marketing_start_date": "20190110"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-422-30)", "package_ndc": "50228-422-30", "marketing_start_date": "20190110"}], "brand_name": "Fluoxetine", "product_id": "50228-422_2c27d964-db05-c709-e063-6294a90a385c", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50228-422", "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": "20190110", "listing_expiration_date": "20261231"}