Package 68382-001-06

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 68382-001-06
Digits Only 6838200106
Product NDC 68382-001
Description

30 TABLET, FILM COATED in 1 BOTTLE (68382-001-06)

Marketing

Marketing Status
Marketed Since 2007-04-13
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c88d98d1-e370-4ad8-869a-603875f276cc", "openfda": {"upc": ["0368382098108", "0368382099105"], "unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["a6bb4f0a-1555-4550-a7a4-99609674b1e7"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-001-01)", "package_ndc": "68382-001-01", "marketing_start_date": "20070413"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-001-05)", "package_ndc": "68382-001-05", "marketing_start_date": "20070413"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68382-001-06)", "package_ndc": "68382-001-06", "marketing_start_date": "20070413"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-001-10)", "package_ndc": "68382-001-10", "marketing_start_date": "20070413"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-001-16)", "package_ndc": "68382-001-16", "marketing_start_date": "20070413"}], "brand_name": "Paroxetine", "product_id": "68382-001_c88d98d1-e370-4ad8-869a-603875f276cc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68382-001", "generic_name": "Paroxetine", "labeler_name": "Zydus Pharmaceuticals USA 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": "20070413", "listing_expiration_date": "20261231"}