Package 70518-2387-2

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 70518-2387-2
Digits Only 7051823872
Product NDC 70518-2387
Product ID 70518-2387_4a15aba9-9e60-26ca-e063-6294a90abf2b
Description

30 POUCH in 1 BOX (70518-2387-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2387-3)

Marketing

Marketing Status
Marketed Since 2021-08-05
Brand paroxetine
Generic paroxetine hydrochloride hemihydrate
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": "4a15aba9-9e60-26ca-e063-6294a90abf2b", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738495"], "spl_set_id": ["4cb9dc05-adb8-4c88-ad40-af8c0df1cafd"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-2387-2)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2387-3)", "package_ndc": "70518-2387-2", "marketing_start_date": "20210805"}], "brand_name": "Paroxetine", "product_id": "70518-2387_4a15aba9-9e60-26ca-e063-6294a90abf2b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "70518-2387", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20191024", "listing_expiration_date": "20271231"}