Package 68788-9074-1

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-9074-1
Digits Only 6878890741
Product NDC 68788-9074
Description

100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-1)

Marketing

Marketing Status
Marketed Since 2007-04-13
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": "0264eeca-5671-466c-96ec-ab81e0c114d1", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495"], "spl_set_id": ["605c1d23-c97c-4ea4-92d0-fed351de9d2e"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-1)", "package_ndc": "68788-9074-1", "marketing_start_date": "20070413"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-3)", "package_ndc": "68788-9074-3", "marketing_start_date": "20070413"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-6)", "package_ndc": "68788-9074-6", "marketing_start_date": "20070413"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-8)", "package_ndc": "68788-9074-8", "marketing_start_date": "20070413"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9074-9)", "package_ndc": "68788-9074-9", "marketing_start_date": "20070413"}], "brand_name": "Paroxetine", "product_id": "68788-9074_0264eeca-5671-466c-96ec-ab81e0c114d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68788-9074", "generic_name": "Paroxetine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20070413", "listing_expiration_date": "20261231"}