Package 42708-092-30

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-092-30
Digits Only 4270809230
Product NDC 42708-092
Product ID 42708-092_465355cb-7d34-1617-e063-6294a90a0ef6
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-092-30)

Marketing

Marketing Status
Marketed Since 2018-03-19
Brand sertraline hydrochloride
Generic sertraline hydrochloride
Sample Package Yes

Linked Drug Pages (1)

SERTRALINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "465355cb-7d34-1617-e063-6294a90a0ef6", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["dc97a895-8c2f-4891-85f3-7f45e2396140"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-092-30)", "package_ndc": "42708-092-30", "marketing_start_date": "20180319"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "42708-092_465355cb-7d34-1617-e063-6294a90a0ef6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-092", "generic_name": "SERTRALINE HYDROCHLORIDE", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE HYDROCHLORIDE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA202825", "marketing_category": "ANDA", "marketing_start_date": "20170209", "listing_expiration_date": "20261231"}