Package 70518-2574-4

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 70518-2574-4
Digits Only 7051825744
Product NDC 70518-2574
Product ID 70518-2574_4a6883b0-36a2-14fa-e063-6294a90a281c
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2574-4)

Marketing

Marketing Status
Marketed Since 2024-10-09
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": "4a6883b0-36a2-14fa-e063-6294a90a281c", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["f52ca1fc-fbf7-4b2b-9e74-975c310b8ce6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2574-4)", "package_ndc": "70518-2574-4", "marketing_start_date": "20241009"}], "brand_name": "Paroxetine", "product_id": "70518-2574_4a6883b0-36a2-14fa-e063-6294a90a281c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2574", "generic_name": "Paroxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA078406", "marketing_category": "ANDA", "marketing_start_date": "20200210", "listing_expiration_date": "20271231"}