Package 60760-683-90

Brand: sertraline

Generic: sertraline
NDC Package

Package Facts

Identity

Package NDC 60760-683-90
Digits Only 6076068390
Product NDC 60760-683
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-683-90)

Marketing

Marketing Status
Marketed Since 2025-09-02
Brand sertraline
Generic sertraline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3dd832b1-cef3-e200-e063-6294a90a8ec3", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["3dd83384-09b5-da46-e063-6394a90a558c"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-683-90)", "package_ndc": "60760-683-90", "marketing_start_date": "20250902"}], "brand_name": "Sertraline", "product_id": "60760-683_3dd832b1-cef3-e200-e063-6294a90a8ec3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-683", "generic_name": "Sertraline", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076465", "marketing_category": "ANDA", "marketing_start_date": "20230223", "listing_expiration_date": "20261231"}