Package 80425-0184-3

Brand: quetiapine fumarate

Generic: quetiapine fumarate
NDC Package

Package Facts

Identity

Package NDC 80425-0184-3
Digits Only 8042501843
Product NDC 80425-0184
Description

90 TABLET, FILM COATED in 1 BOTTLE (80425-0184-3)

Marketing

Marketing Status
Marketed Since 2016-07-01
Brand quetiapine fumarate
Generic quetiapine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99a670-af36-299d-e063-6294a90a05d2", "openfda": {"unii": ["2S3PL1B6UJ"], "rxcui": ["616487"], "spl_set_id": ["d323b6c0-55fa-6caa-e053-2a95a90a3cff"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0184-3)", "package_ndc": "80425-0184-3", "marketing_start_date": "20160701"}], "brand_name": "Quetiapine Fumarate", "product_id": "80425-0184_2a99a670-af36-299d-e063-6294a90a05d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "80425-0184", "generic_name": "Quetiapine Fumarate", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quetiapine Fumarate", "active_ingredients": [{"name": "QUETIAPINE FUMARATE", "strength": "50 mg/1"}], "application_number": "ANDA202674", "marketing_category": "ANDA", "marketing_start_date": "20160701", "listing_expiration_date": "20261231"}