Package 0615-8174-39

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 0615-8174-39
Digits Only 0615817439
Product NDC 0615-8174
Product ID 0615-8174_34c4cb21-d274-4d85-90f4-df09a9beffd8
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8174-39)

Marketing

Marketing Status
Marketed Since 2018-03-05
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Paroxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34c4cb21-d274-4d85-90f4-df09a9beffd8", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738495", "1738503", "1738511"], "spl_set_id": ["c3b2ce88-6f09-4f7b-ac73-93dca84aa3b8"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8174-39)", "package_ndc": "0615-8174-39", "marketing_start_date": "20180305"}], "brand_name": "Paroxetine", "product_id": "0615-8174_34c4cb21-d274-4d85-90f4-df09a9beffd8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0615-8174", "generic_name": "Paroxetine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}