Package 50090-7701-0

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7701-0
Digits Only 5009077010
Product NDC 50090-7701
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7701-0)

Marketing

Marketing Status
Marketed Since 2025-10-13
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": "65bda6eb-aa0c-4e22-aad6-09dc734adf85", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["1b069fd8-26b9-459e-abfb-de28c012ddcb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7701-0)", "package_ndc": "50090-7701-0", "marketing_start_date": "20251013"}], "brand_name": "Sertraline Hydrochloride", "product_id": "50090-7701_65bda6eb-aa0c-4e22-aad6-09dc734adf85", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7701", "generic_name": "Sertraline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077670", "marketing_category": "ANDA", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}