Package 76282-214-30

Brand: sertraline

Generic: sertraline
NDC Package

Package Facts

Identity

Package NDC 76282-214-30
Digits Only 7628221430
Product NDC 76282-214
Description

30 TABLET, FILM COATED in 1 BOTTLE (76282-214-30)

Marketing

Marketing Status
Marketed Since 2012-08-20
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": "5c34aa64-3f25-4d6e-8fbb-98aa3688f72d", "openfda": {"upc": ["0376282214306", "0376282212302", "0376282213309"], "unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["2dac437f-b5ef-42dd-aa0b-1f4b9b45ef43"], "manufacturer_name": ["Exelan Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76282-214-01)", "package_ndc": "76282-214-01", "marketing_start_date": "20120820"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76282-214-05)", "package_ndc": "76282-214-05", "marketing_start_date": "20120820"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (76282-214-18)", "package_ndc": "76282-214-18", "marketing_start_date": "20120820"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76282-214-30)", "package_ndc": "76282-214-30", "marketing_start_date": "20120820"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76282-214-60)", "package_ndc": "76282-214-60", "marketing_start_date": "20120820"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76282-214-90)", "package_ndc": "76282-214-90", "marketing_start_date": "20120820"}], "brand_name": "SERTRALINE", "product_id": "76282-214_5c34aa64-3f25-4d6e-8fbb-98aa3688f72d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "76282-214", "generic_name": "Sertraline", "labeler_name": "Exelan Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA077397", "marketing_category": "ANDA", "marketing_start_date": "20120820", "listing_expiration_date": "20261231"}