Package 70518-4543-0

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4543-0
Digits Only 7051845430
Product NDC 70518-4543
Product ID 70518-4543_47cc805c-cbf9-f3d0-e063-6294a90aa1e8
Description

30 CAPSULE in 1 BLISTER PACK (70518-4543-0)

Marketing

Marketing Status
Marketed Since 2026-01-07
Brand fluoxetine
Generic fluoxetine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47cc805c-cbf9-f3d0-e063-6294a90aa1e8", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310385"], "spl_set_id": ["b8666383-462d-4a21-8f49-1d572da386d1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4543-0)", "package_ndc": "70518-4543-0", "marketing_start_date": "20260107"}], "brand_name": "Fluoxetine", "product_id": "70518-4543_47cc805c-cbf9-f3d0-e063-6294a90aa1e8", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4543", "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": "ANDA078619", "marketing_category": "ANDA", "marketing_start_date": "20260107", "listing_expiration_date": "20271231"}