Package 70518-3483-0

Brand: fluoxetine

Generic: fluoxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3483-0
Digits Only 7051834830
Product NDC 70518-3483
Description

30 CAPSULE in 1 BLISTER PACK (70518-3483-0)

Marketing

Marketing Status
Marketed Since 2022-08-17
Brand fluoxetine
Generic fluoxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a9d64f1-ea44-5bc6-e063-6394a90a9e15", "openfda": {"unii": ["I9W7N6B1KJ"], "rxcui": ["310384"], "spl_set_id": ["8b8fe00e-7a2f-486b-9b72-465a494d8939"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3483-0)", "package_ndc": "70518-3483-0", "marketing_start_date": "20220817"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3483-1)", "package_ndc": "70518-3483-1", "marketing_start_date": "20220920"}], "brand_name": "Fluoxetine", "product_id": "70518-3483_3a9d64f1-ea44-5bc6-e063-6394a90a9e15", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-3483", "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": "ANDA204597", "marketing_category": "ANDA", "marketing_start_date": "20220817", "listing_expiration_date": "20261231"}