Package 62135-543-90

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 62135-543-90
Digits Only 6213554390
Product NDC 62135-543
Description

90 TABLET, FILM COATED in 1 BOTTLE (62135-543-90)

Marketing

Marketing Status
Marketed Since 2023-04-11
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4687b126-663e-b64a-e063-6294a90affa1", "openfda": {"upc": ["0362135544904", "0362135542900", "0362135541903", "0362135543907"], "unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["69699d40-4a64-4337-8664-e4e093437fbf"], "manufacturer_name": ["Chartwell RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-543-90)", "package_ndc": "62135-543-90", "marketing_start_date": "20230411"}], "brand_name": "PAROXETINE", "product_id": "62135-543_4687b126-663e-b64a-e063-6294a90affa1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "62135-543", "generic_name": "PAROXETINE", "labeler_name": "Chartwell RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "30 mg/1"}], "application_number": "ANDA211248", "marketing_category": "ANDA", "marketing_start_date": "20211102", "listing_expiration_date": "20261231"}