Package 54838-523-40

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54838-523-40
Digits Only 5483852340
Product NDC 54838-523
Product ID 54838-523_bda5665d-4bcd-4426-9397-e438485d0d29
Description

120 mL in 1 BOTTLE, PLASTIC (54838-523-40)

Marketing

Marketing Status
Marketed Since 2009-08-27
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": "bda5665d-4bcd-4426-9397-e438485d0d29", "openfda": {"upc": ["0354838523409"], "unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["c856d72f-4a1a-4f75-ae54-c4ac83ddcfa1"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, PLASTIC (54838-523-40)", "package_ndc": "54838-523-40", "marketing_start_date": "20090827"}], "brand_name": "Fluoxetine", "product_id": "54838-523_bda5665d-4bcd-4426-9397-e438485d0d29", "dosage_form": "LIQUID", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "54838-523", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA077849", "marketing_category": "ANDA", "marketing_start_date": "20090827", "listing_expiration_date": "20261231"}