Package 68071-1740-1

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 68071-1740-1
Digits Only 6807117401
Product NDC 68071-1740
Product ID 68071-1740_1d5082fe-1cd7-39a8-e063-6294a90ac90f
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-1740-1)

Marketing

Marketing Status
Marketed Since 2017-08-18
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": "1d5082fe-1cd7-39a8-e063-6294a90ac90f", "openfda": {"upc": ["0368071174014"], "unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["570a9f0d-04fb-2922-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-1740-1)", "package_ndc": "68071-1740-1", "marketing_start_date": "20170818"}], "brand_name": "Paroxetine", "product_id": "68071-1740_1d5082fe-1cd7-39a8-e063-6294a90ac90f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68071-1740", "generic_name": "Paroxetine", "labeler_name": "NuCare Pharmaceuticals,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": "20261231"}