Package 70518-4425-0

Brand: sertraline

Generic: sertraline
NDC Package

Package Facts

Identity

Package NDC 70518-4425-0
Digits Only 7051844250
Product NDC 70518-4425
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4425-0)

Marketing

Marketing Status
Marketed Since 2025-08-05
Brand sertraline
Generic sertraline
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4040f632-2056-31c0-e063-6294a90aeb27", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312940"], "spl_set_id": ["7efc1dd5-8671-4bed-9c16-ef6b9f36afc4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4425-0)", "package_ndc": "70518-4425-0", "marketing_start_date": "20250805"}], "brand_name": "Sertraline", "product_id": "70518-4425_4040f632-2056-31c0-e063-6294a90aeb27", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4425", "generic_name": "Sertraline", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA076465", "marketing_category": "ANDA", "marketing_start_date": "20250805", "listing_expiration_date": "20261231"}