Package 70518-4420-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4420-0
Digits Only 7051844200
Product NDC 70518-4420
Product ID 70518-4420_3b8e4b88-18cd-0821-e063-6294a90a8396
Description

30 CAPSULE in 1 BLISTER PACK (70518-4420-0)

Marketing

Marketing Status
Marketed Since 2025-07-31
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": "3b8e4b88-18cd-0821-e063-6294a90a8396", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["a08dadff-f209-48dc-b597-6f085be13640"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4420-0)", "package_ndc": "70518-4420-0", "marketing_start_date": "20250731"}], "brand_name": "Fluoxetine", "product_id": "70518-4420_3b8e4b88-18cd-0821-e063-6294a90a8396", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4420", "generic_name": "Fluoxetine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}