Package 71656-089-04

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 71656-089-04
Digits Only 7165608904
Product NDC 71656-089
Product ID 71656-089_38420669-08b4-a3e4-e063-6294a90a4573
Description

120 mL in 1 BOTTLE (71656-089-04)

Marketing

Marketing Status
Marketed Since 2025-06-20
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": "38420669-08b4-a3e4-e063-6294a90a4573", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310386"], "spl_set_id": ["4527c502-b28c-449f-ad2d-7daf21563cfa"], "manufacturer_name": ["Saptalis Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (71656-089-04)", "package_ndc": "71656-089-04", "marketing_start_date": "20250620"}], "brand_name": "FLUOXETINE", "product_id": "71656-089_38420669-08b4-a3e4-e063-6294a90a4573", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71656-089", "generic_name": "FLUOXETINE", "labeler_name": "Saptalis Pharmaceuticals, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUOXETINE", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA075525", "marketing_category": "ANDA", "marketing_start_date": "20250620", "listing_expiration_date": "20261231"}