Package 70518-4428-0

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4428-0
Digits Only 7051844280
Product NDC 70518-4428
Product ID 70518-4428_3bb88af7-5af2-8a09-e063-6294a90a61cf
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4428-0)

Marketing

Marketing Status
Marketed Since 2025-08-06
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": "3bb88af7-5af2-8a09-e063-6294a90a61cf", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["248642"], "spl_set_id": ["58b39e6a-3aae-4551-b081-586a4506aef2"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4428-0)", "package_ndc": "70518-4428-0", "marketing_start_date": "20250806"}], "brand_name": "Fluoxetine", "product_id": "70518-4428_3bb88af7-5af2-8a09-e063-6294a90a61cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4428", "generic_name": "Fluoxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA213286", "marketing_category": "ANDA", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}