Package 68071-2535-9

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 68071-2535-9
Digits Only 6807125359
Product NDC 68071-2535
Product ID 68071-2535_49dcbbe1-ceb2-c8eb-e063-6394a90a9c5e
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-2535-9)

Marketing

Marketing Status
Marketed Since 2026-02-02
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Paroxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49dcbbe1-ceb2-c8eb-e063-6394a90a9c5e", "openfda": {"upc": ["0368071253597"], "unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["49dc055c-faef-0be3-e063-6394a90a934f"], "manufacturer_name": ["NuCare Pharamceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2535-9)", "package_ndc": "68071-2535-9", "marketing_start_date": "20260202"}], "brand_name": "Paroxetine", "product_id": "68071-2535_49dcbbe1-ceb2-c8eb-e063-6394a90a9c5e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-2535", "generic_name": "Paroxetine", "labeler_name": "NuCare Pharamceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20070413", "listing_expiration_date": "20271231"}