Package 51655-265-26

Brand: sertraline hydrochloride

Generic: sertraline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-265-26
Digits Only 5165526526
Product NDC 51655-265
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-265-26)

Marketing

Marketing Status
Marketed Since 2020-06-08
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": "48e6c26d-a3cb-62e6-e063-6394a90a44e3", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["312941"], "spl_set_id": ["ab1bb71f-936d-cb40-e053-2a95a90a08bb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-265-26)", "package_ndc": "51655-265-26", "marketing_start_date": "20200608"}], "brand_name": "Sertraline Hydrochloride", "product_id": "51655-265_48e6c26d-a3cb-62e6-e063-6394a90a44e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "51655-265", "generic_name": "Sertraline Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "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": "20200608", "listing_expiration_date": "20271231"}