Package 72162-2358-9

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 72162-2358-9
Digits Only 7216223589
Product NDC 72162-2358
Product ID 72162-2358_c6a22c4a-3353-418e-8cda-6cf6b46f3544
Description

90 TABLET, FILM COATED in 1 BOTTLE (72162-2358-9)

Marketing

Marketing Status
Marketed Since 2024-06-28
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": "c6a22c4a-3353-418e-8cda-6cf6b46f3544", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["ac6ea24f-a9f3-4413-8c3a-9e2e4ca93c0f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-2358-9)", "package_ndc": "72162-2358-9", "marketing_start_date": "20240628"}], "brand_name": "Paroxetine", "product_id": "72162-2358_c6a22c4a-3353-418e-8cda-6cf6b46f3544", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2358", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}