Package 70518-1174-2

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1174-2
Digits Only 7051811742
Product NDC 70518-1174
Product ID 70518-1174_48bff792-4d3d-cb61-e063-6394a90acbea
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (70518-1174-2)

Marketing

Marketing Status
Marketed Since 2025-08-27
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": "48bff792-4d3d-cb61-e063-6394a90acbea", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["32afb28a-dc4c-4a7e-9701-1825f805e7df"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-1174-2)", "package_ndc": "70518-1174-2", "marketing_start_date": "20250827"}], "brand_name": "Fluoxetine", "product_id": "70518-1174_48bff792-4d3d-cb61-e063-6394a90acbea", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1174", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20271231"}