Package 70518-1460-1

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1460-1
Digits Only 7051814601
Product NDC 70518-1460
Product ID 70518-1460_4900bb35-ed0a-8189-e063-6294a90a9c82
Description

100 POUCH in 1 BOX (70518-1460-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1460-2)

Marketing

Marketing Status
Marketed Since 2020-11-09
Brand paroxetine
Generic paroxetine hydrochloride
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": "4900bb35-ed0a-8189-e063-6294a90a9c82", "openfda": {"unii": ["3I3T11UD2S"], "rxcui": ["1738503"], "spl_set_id": ["8e176ff2-ed3a-4909-94e1-6b9a3581a621"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-1460-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-1460-2)", "package_ndc": "70518-1460-1", "marketing_start_date": "20201109"}], "brand_name": "PAROXETINE", "product_id": "70518-1460_4900bb35-ed0a-8189-e063-6294a90a9c82", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-1460", "generic_name": "paroxetine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE ANHYDROUS", "strength": "30 mg/1"}], "application_number": "ANDA075356", "marketing_category": "ANDA", "marketing_start_date": "20181004", "listing_expiration_date": "20271231"}