Package 72162-2407-3

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2407-3
Digits Only 7216224073
Product NDC 72162-2407
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-2407-3)

Marketing

Marketing Status
Marketed Since 2024-10-21
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": "71094aa2-232a-452f-b92a-47ccab669523", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["9f1d5689-3bf1-431c-9ea2-9e37217ecf40"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2407-3)", "package_ndc": "72162-2407-3", "marketing_start_date": "20241021"}], "brand_name": "Sertraline Hydrochloride", "product_id": "72162-2407_71094aa2-232a-452f-b92a-47ccab669523", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2407", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sertraline Hydrochloride", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}