Package 70518-4157-1
Brand: sertraline hydrochloride
Generic: sertraline hydrochloridePackage Facts
Identity
Package NDC
70518-4157-1
Digits Only
7051841571
Product NDC
70518-4157
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4157-1)
Marketing
Marketing Status
Brand
sertraline hydrochloride
Generic
sertraline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40945805-6f2c-74a1-e063-6394a90a04a3", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["9d49e2cb-a852-403d-b92b-e7d3fa88032c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4157-1)", "package_ndc": "70518-4157-1", "marketing_start_date": "20240918"}], "brand_name": "Sertraline hydrochloride", "product_id": "70518-4157_40945805-6f2c-74a1-e063-6394a90a04a3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-4157", "generic_name": "Sertraline hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA078403", "marketing_category": "ANDA", "marketing_start_date": "20240813", "listing_expiration_date": "20261231"}