Package 16714-182-04

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-182-04
Digits Only 1671418204
Product NDC 16714-182
Description

1000 TABLET, FILM COATED in 1 BOTTLE (16714-182-04)

Marketing

Marketing Status
Marketed Since 2007-07-25
Brand paroxetine
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e3542cb-82a1-4a53-b814-55cfa4075ba6", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["118320de-0632-4139-8b13-7428b41da0ac"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16714-182-01)", "package_ndc": "16714-182-01", "marketing_start_date": "20070725"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16714-182-02)", "package_ndc": "16714-182-02", "marketing_start_date": "20070725"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-182-03)", "package_ndc": "16714-182-03", "marketing_start_date": "20070725"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16714-182-04)", "package_ndc": "16714-182-04", "marketing_start_date": "20070725"}], "brand_name": "Paroxetine", "product_id": "16714-182_0e3542cb-82a1-4a53-b814-55cfa4075ba6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "16714-182", "generic_name": "Paroxetine Hydrochloride", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA078406", "marketing_category": "ANDA", "marketing_start_date": "20070725", "listing_expiration_date": "20261231"}