Package 71335-0321-4

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 71335-0321-4
Digits Only 7133503214
Product NDC 71335-0321
Description

180 TABLET, FILM COATED in 1 BOTTLE (71335-0321-4)

Marketing

Marketing Status
Marketed Since 2021-12-27
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": "12cfc765-bf13-4a46-8985-36e31c75fab9", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738503"], "spl_set_id": ["0a0f8897-2099-4038-9b96-ed9c4f084018"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0321-1)", "package_ndc": "71335-0321-1", "marketing_start_date": "20180212"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0321-2)", "package_ndc": "71335-0321-2", "marketing_start_date": "20211227"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0321-3)", "package_ndc": "71335-0321-3", "marketing_start_date": "20180517"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0321-4)", "package_ndc": "71335-0321-4", "marketing_start_date": "20211227"}], "brand_name": "Paroxetine", "product_id": "71335-0321_12cfc765-bf13-4a46-8985-36e31c75fab9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71335-0321", "generic_name": "Paroxetine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "30 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20070413", "listing_expiration_date": "20261231"}