Package 60760-988-90

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-988-90
Digits Only 6076098890
Product NDC 60760-988
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-988-90)

Marketing

Marketing Status
Marketed Since 2024-08-15
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": "43d00c03-05b2-93d9-e063-6294a90ae261", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["1fcd3f6d-a71f-b131-e063-6394a90a4b26"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-988-90)", "package_ndc": "60760-988-90", "marketing_start_date": "20240815"}], "brand_name": "Sertraline hydrochloride", "product_id": "60760-988_43d00c03-05b2-93d9-e063-6294a90ae261", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60760-988", "generic_name": "Sertraline hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20230515", "listing_expiration_date": "20261231"}