Package 70518-4171-0

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4171-0
Digits Only 7051841710
Product NDC 70518-4171
Product ID 70518-4171_3fb92496-8093-443f-e063-6394a90af23c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4171-0)

Marketing

Marketing Status
Marketed Since 2024-08-28
Brand sertraline hydrochloride
Generic sertraline hydrochloride
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": "3fb92496-8093-443f-e063-6394a90af23c", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312940"], "spl_set_id": ["455c8416-c878-4283-a42f-4df896870a4e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4171-0)", "package_ndc": "70518-4171-0", "marketing_start_date": "20240828"}], "brand_name": "Sertraline hydrochloride", "product_id": "70518-4171_3fb92496-8093-443f-e063-6394a90af23c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4171", "generic_name": "Sertraline hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA078403", "marketing_category": "ANDA", "marketing_start_date": "20240828", "listing_expiration_date": "20261231"}