Package 70518-4429-0

Brand: fluoxetine

Generic: fluoxetine
NDC Package

Package Facts

Identity

Package NDC 70518-4429-0
Digits Only 7051844290
Product NDC 70518-4429
Product ID 70518-4429_3bdeda64-6772-f53c-e063-6294a90a3d6a
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4429-0)

Marketing

Marketing Status
Marketed Since 2025-08-08
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": "3bdeda64-6772-f53c-e063-6294a90a3d6a", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["313990"], "spl_set_id": ["ac1651cc-4a2e-47cf-8a7e-be7ddcaf9f31"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4429-0)", "package_ndc": "70518-4429-0", "marketing_start_date": "20250808"}], "brand_name": "Fluoxetine", "product_id": "70518-4429_3bdeda64-6772-f53c-e063-6294a90a3d6a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4429", "generic_name": "Fluoxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213286", "marketing_category": "ANDA", "marketing_start_date": "20250808", "listing_expiration_date": "20261231"}