Package 42708-124-30

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package Sample

Package Facts

Identity

Package NDC 42708-124-30
Digits Only 4270812430
Product NDC 42708-124
Product ID 42708-124_459c0f76-6c95-c236-e063-6394a90ac254
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-124-30)

Marketing

Marketing Status
Marketed Since 2018-05-24
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": "459c0f76-6c95-c236-e063-6394a90ac254", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["664d1744-7b1d-43e2-98ba-1b0e69d75840"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-124-30)", "package_ndc": "42708-124-30", "marketing_start_date": "20180524"}], "brand_name": "Sertraline Hydrochloride", "product_id": "42708-124_459c0f76-6c95-c236-e063-6394a90ac254", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "42708-124", "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": "ANDA077206", "marketing_category": "ANDA", "marketing_start_date": "20070206", "listing_expiration_date": "20261231"}