Package 70518-0003-0

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 70518-0003-0
Digits Only 7051800030
Product NDC 70518-0003
Product ID 70518-0003_4b1bfe2a-c10f-2cef-e063-6394a90a8ea4
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0003-0)

Marketing

Marketing Status
Marketed Since 2016-11-23
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": "4b1bfe2a-c10f-2cef-e063-6394a90a8ea4", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["bc0efd3b-c6b9-4ed0-b517-6e57e4700b7b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0003-0)", "package_ndc": "70518-0003-0", "marketing_start_date": "20161123"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0003-1)", "package_ndc": "70518-0003-1", "marketing_start_date": "20220601"}], "brand_name": "Paroxetine", "product_id": "70518-0003_4b1bfe2a-c10f-2cef-e063-6394a90a8ea4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-0003", "generic_name": "Paroxetine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20161123", "listing_expiration_date": "20271231"}