Package 71610-433-15

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-433-15
Digits Only 7161043315
Product NDC 71610-433
Description

15 TABLET, FILM COATED in 1 BOTTLE (71610-433-15)

Marketing

Marketing Status
Marketed Since 2020-06-16
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": "7c2f1809-97f9-4942-a4f0-5fe016dd709a", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312938"], "spl_set_id": ["ccb264a4-5d50-4317-a67e-ba6daa2b8297"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71610-433-15)", "package_ndc": "71610-433-15", "marketing_start_date": "20200616"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "71610-433_7c2f1809-97f9-4942-a4f0-5fe016dd709a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-433", "generic_name": "sertraline hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE HYDROCHLORIDE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "NDA019839", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190812", "listing_expiration_date": "20261231"}