Package 72189-492-30

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 72189-492-30
Digits Only 7218949230
Product NDC 72189-492
Product ID 72189-492_2c4e39ee-1b27-61c5-e063-6394a90aeef5
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-492-30)

Marketing

Marketing Status
Marketed Since 2023-06-21
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": "2c4e39ee-1b27-61c5-e063-6394a90aeef5", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["fea936a5-fdeb-e4fb-e053-6294a90a8995"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-492-30)", "package_ndc": "72189-492-30", "marketing_start_date": "20230621"}], "brand_name": "Paroxetine", "product_id": "72189-492_2c4e39ee-1b27-61c5-e063-6394a90aeef5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72189-492", "generic_name": "Paroxetine", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20230621", "listing_expiration_date": "20261231"}